Hypertrichosis lanuginosa congenitaQ84.2
Synonym(s)
Congenital generalized hypertrichosis; Congenital generalized hypertrichosis lanuginosa; Congenital hypertrichosis lanuginosa; hypertrichosis universalis
DefinitionThis section has been translated automatically.
Rare, generalized, autosomal dominant inherited, congenital, increased body hair, which is monoorganically limited to the integument, but also appears together with other organ involvement.
Clinical featuresThis section has been translated automatically.
The dermatological findings are as follows: fine, non-markless, light to silver-grey hairs of up to 20 cm in length are found all over the body.
TherapyThis section has been translated automatically.
Only shaving or epilating by means of laser techniques can be considered.
LiteratureThis section has been translated automatically.
- Bou-Assi E et al.(2016) Neonatal Cutis Laxa and Hypertrichosis Lanuginosa in Sotos Syndrome. Pediatric dermatol 33:e351-e352.
- Canún S et al (2003) Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity. At J Med Genet A 116A: 278-283.
- Chen W et al (2015) Congenital generalized hypertrichosis terminalis: a proposed classification and a plea to avoid the ambiguous term "Ambras syndrome". Eur J Dermatol 25:223-227.
- Gilhooley E et al (2017) FOXN1 Duplication and Congenital Hypertrichosis. Pediatric Dermatol 34:e77-e79.
- Salas-Alanis JC et al (2014) Hypertrichosis lanuginosa congenita treated with diode laser epilation during infancy. Pediatric Dermatol 31:529-530.
- Shah IH et al. (2018) Congenital hypertrichosis lanuginosa. Indian J Dermatol Venereol Leprol 84:248.