What can cause hypertrichosis?

Minoxidil penicillamine I-cell disease Donohue syndrome variegate porphyria Hepatoerythropoietic porphyria porphyria ciclosporin polymyositis paraneoplastic syndrome Hurler syndrome porphyria cutanea tarda POEMS syndrome Schinzel-Giedion midface-retraction syndrome Gangliosidosis GM1, type 1 Barber-Say syndrome Ramon syndrome Rolland-Desbuquois dyssegmental dysplasia Erythrokeratoderma variabilis Pigmented hairy epidermal nevus Hypertrichosis lanuginosa, congenital Hereditary gingival fibromatosis Congenital generalized lipodystrophy type 2 Gorlin-Chaudhry-Moss syndrome Glucocorticoids, topical Hypertrichotic osteochondrodysplasia Congenital generalized lipodystrophy type 1.

Hurler syndrome Alpha-L-iduronidase deficiency (hurler syndrome) () wikipedia porphyria cutanea tarda porphyria cutanea tarda, a most common subtype of porphyria wikipedia POEMS syndrome POEMS syndrome, a rare medical syndrome named for its main clinically recognizable features: Polyneuropathy, Organomegaly, Endocrinopathy /Edema, M-protein and Skin abnormalities wikipedia Schinzel-Giedion midface-retraction syndrome Schinzel-Giedion syndrome, the congenital neurodegenerative terminal syndrome wikipedia Gangliosidosis GM1, type 1 Gangliosidosis GM1, type 1, the cause and medical condition with Mesh code "D016537" and DiseasesDB code "34496" Barber-Say syndrome Barber-Say syndrome, the cause and medical concept with DiseasesDB code "33294" Ramon syndrome Ramon syndrome (a slowly progressive syndrome involving cherubism, maxillary fibrous dysplasia, gingival enlargement, radiolucent lesions of the jaws, seizures, delayed mental development, stunted growth, and other defects) Rolland-Desbuquois dyssegmental dysplasia Rolland-Desbuquois dyssegmental dysplasia, the cause and medical concept with DiseasesDB code "32474" Erythrokeratoderma variabilis Erythrokeratoderma variabilis (an autosomal dominant skin disease characterized by transient and variable noninflammatory erythema and hyperkeratosis) Pigmented hairy epidermal nevus Pigmented hairy epidermal nevus, the cause and medical condition with DiseasesDB code "31362" Hypertrichosis lanuginosa, congenital Hypertrichosis lanuginosa, congenital, the cause and medical concept with DiseasesDB code "31317" Hereditary gingival fibromatosis Hereditary gingival fibromatosis, the cause and medical concept with DiseasesDB code "30743" Congenital generalized lipodystrophy type 2 Congenital generalized lipodystrophy type 2 (a type of diabetes mellitus that is characterized by severe insulin resistance and lipodystrophy) Gorlin-Chaudhry-Moss syndrome Gorlin-Chaudhry-Moss syndrome, the cause and medical concept with DiseasesDB code "29899" Glucocorticoids, topical Glucocorticoids, topical (any synthetic steroid derivative exhibiting the same function as the naturally occurring corticosteroid hormone, formulated for topical application) Hypertrichotic osteochondrodysplasia Hypertrichotic osteochondrodysplasia (heart enlargement, hypertrichosis, osteochondrodysplasia, large body, and borderline or mild mental retardation are the main characteristics of this syndrome) Congenital generalized lipodystrophy type 1 Congenital generalized lipodystrophy type 1 (it is caused by mutations of gene encoding 1-acylglycerol-3-phosphate O-acyltransferase-2 (agpat2)).

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