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Afecţiunea – hypertrichosis universalis – se manifestă prin creşterea excesivă a părului pe întreg corpul.
Este una dintre cele mai rare afecţiuni medicale din lume, de care suferă doar un om dintr-un miliard. Reuters a publicat duminică pe o reţea de socializare fotografia micuţei Mandira din Nepal care suferă de teribila boală genetică. Aceeaşi afecţiune are şi fratele ei, Niraj Budhathoki, în vârstă de 12 de ani din Nepal, dar şi sora lui mai mare, Manjura. Mama lor are aceeaşi boală rară şi toţi urmează un tratament cu laser pentru a reduce simptomele bolii.
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Foto captura Facebook//Reuters
Mama lui Niraj, Devi Budhathoki, spune că ea este prima din familia ei care suferă de “sindromul vârcolacului” .
Boala care afectează un om dintr-un miliard. Cum se manifestă ”sindromul vârcolacului”. GALERIE FOTO
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