{"id":11450,"date":"2025-07-26T18:27:05","date_gmt":"2025-07-26T16:27:05","guid":{"rendered":"https:\/\/valintermed.com\/?p=11450"},"modified":"2025-07-26T18:27:05","modified_gmt":"2025-07-26T16:27:05","slug":"vrozhdennyy-lanuginoznyy-gipertrihoz","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/congenital-languinous-hypertrihoz\/","title":{"rendered":"Congenital lanuginous hypertrichosis"},"content":{"rendered":"
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Congenital hypertrichosis lanuginosa is a rare genetic disorder characterized by excessive hair growth on the body and face of newborns, especially in the lanuginous area. The condition is associated with abnormal mutations in certain genes that are responsible for the normal development of hair follicles. Patients with the disorder have increased hair fiber activity even in areas of the skin that are normally hairless. The disorder can present in a variety of forms, from mild hypertrichosis affecting only small areas to severe forms with large areas of baldness along with excessive hair growth. It has significant clinical, aesthetic, and psychological consequences for patients and their families, as it can lead to significant social and emotional difficulties.<\/p>\n

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