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  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_004.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_005.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_011.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_015.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_014.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_016.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_009.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_012.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_002.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_008.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_007.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_013.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_017.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_001.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_003.jpg
  • EXCLUSIVE: Hugh Hefner's son, Marston is seen here the day after his father died at age 91. He left the famed Playboy mansion for a little while to visit a hair salon 'Benjamin with Nagin Zand' in Beverly Hills. 28 Sep 2017 Pictured: Marston Hefner. Photo credit: APEX / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91605_006.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_002.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_006.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_007.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_005.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_008.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_003.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_004.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_011.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_010.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_001.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_009.jpg