Childhood hypertrichosis: diagnosis and management.

Author:

Baumeister F A,Schwarz H P,Stengel-Rutkowski S

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. Prepubertal hypertrichosis: normal or abnormal?;Barth, J.H.; Wilkinson, J.D.; Dawber, R.P.R.;Arch Dis Child,1988

2. Dermatology,1991

3. Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;VA, Mc Kusick,1992

4. POSSUM (pictures of standard syndromes and undiagnosed malformations);Bankier, A.; Ayme, S.; Sillence, D.O.; Kozlowski, K.; Rogers, M.,1991

5. B-galactosidase deficiency (GM1 gangliosidosis, galactosialidosis, and Morquio syndrome type B); ganglioside sialidase deficiency (mucolipidosis IV);O'Brien, J.S.,1989

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1. Approach to inherited hypertrichosis: A brief review;Indian Journal of Dermatology, Venereology and Leprology;2021-07-29

2. Generalized hypertrichosis syndromes in Mexico;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2020-12

3. A Rare Case of Gingival Fibromatosis Associated with Hypertrichosis and a Dysmorphic Face;Journal of Clinical Pediatric Dentistry;2011-04-01

4. Disorders of Hair;Rook's Textbook of Dermatology;2010-05-06

5. Hypertrichosis Cubiti: Another Case of a Well-Recognized but Under-Reported Entity;Pediatric Dermatology;2010-05

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