Nepalese Family With A Rare Disease - Alternative View

Nepalese Family With A Rare Disease - Alternative View
Nepalese Family With A Rare Disease - Alternative View

Video: Nepalese Family With A Rare Disease - Alternative View

Video: Nepalese Family With A Rare Disease - Alternative View
Video: Living with a rare disease: A story of two siblings 2024, September
Anonim

Devi Budhathoki, 37, and her children Manjura, 13, Niraj, 12, and Mandira, 5, suffer from a rare werewolf syndrome characterized by increased hairiness.

In search of a cure, they came from a distant mountainous Nepalese village to the capital city of Kathmandu. They hope that at least someone will help them here. A similar werewolf syndrome was recently widely reported in the press by the example of the Sangdi family from India. There, only women suffered from a rare disease.

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Due to hypertrichosis, the mother, her son and two daughters have particularly strong hair growth in the area of the eyebrows, cheeks and forehead. At the hospital in Kathmandu, the family was examined by the doctor Shankar Man Rai and said that it was all about a genetic abnormality that is inherited. Then he reassured the mother of the family, saying that a good course of laser hair removal could help her and her children.

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Davy was extremely happy about this. Most of all, she would like her children to finally stop being teased and insulted because of their unusual appearance. 12-year-old Neeraj was especially worried about this.