Por su parte, en la hipertricosis congénita los afectados poseen un vello más bien grueso, especialmente en el área de la cara. J R Soc Med ;89 (7) PubMedGoogle Scholar. 6. Mendiratta VHarjai BGupta T Hypertrichosis lanuginosa congenita. Pediatr Dermatol ;25 (4). Hipertricosis Congénita Hipertricosis Congenita ¿En que consiste? La hipertricosis, o síndrome del hombre lobo, es una enfermedad muy.
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Hipertricosis. by Maria Martinez on Prezi
Copyright American Medical Association. Congenital hypertrichosis lanuginosa CHL is a rare disorder, with fewer than 50 cases reported in the literature. It is characterized by excessive lanugo hair present at birth covering the hioertricosis body surface except the mucosae, palms, and soles.
It is considered to be an autosomal dominant disorder, but sporadic presentations are also reported.
We report herein CHL in a father and son. A month-old boy presented with a history of excessive hairiness since birth that increased progressively during infancy.
At presentation, he had excess long, dark blond, silky hair on the face, ears, trunk Figure 1and limbs Figure 2. There was hipertircosis of the hairiness over the lumbosacral spine and sacrum Figure 1. His eyebrows were very thick and coarse, his eyelashes surprisingly long. The face was coarse, and there was a small sacral dimple.
There were no indications of skeletal abnormalities.
Congenital Hypertrichosis Lanuginosa in a Father and Son
Findings of ophthalmologic and stomatologic examinations were normal. Extensive laboratory analyses, including endocrinologic and metabolic evaluations, revealed no abnormalities. His karyotype was normal. Family history revealed that his father had also been unusually hairy during infancy. The father experienced severe hipertricozis caries and wore complete dental prostheses by age 27 years. The father was observed to have coarse eyebrows and long eyelashes at the time of his son’s evaluation.
De Raeve L, Keymolen K. Congenital Hypertrichosis Lanuginosa in a Father and Son.
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