Literature DB >> 18340416

[Hypertrichosis].

R M Trüeb1.   

Abstract

Hypertrichosis denotes growth of hair on any part of the body in excess of the amount usually present in persons of the same age, race, and sex, excluding androgen-dependent hair growth. Hypertrichosis may be an isolated finding or associated with a syndrome, be associated with additional congenital anomalies or a marker for systemic disease. In order to diagnose it accurately, the age of onset, type, localization and pattern of hair growth, associated disorders, medications and perhaps associated anomalies and family history should be considered. Even though hypertrichosis usually has limited medical significance, it often causes cosmetic embarrassment, often resulting in a significant emotional burden. Treatment options are available, though limited in terms of efficacy and patient satisfaction. No single method of hair removal is appropriate for all body locations and patients, and the one adopted will depend on the type, area, and amount of excessive hair growth, as well as on the age, sex, and personal preference of the patient. Patients with hypertrichosis should be adequately advised of the treatment modalities. These include cosmetic procedures (bleaching, trimming, shaving, plucking, waxing, chemical epilatories, electrosurgical epilation), and hair removal using light sources and lasers.

Entities:  

Mesh:

Year:  2008        PMID: 18340416     DOI: 10.1007/s00105-008-1489-z

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  24 in total

Review 1.  Lymphedema-distichiasis syndrome: report of a case and review.

Authors:  S M Johnson; J M Kincannon; T D Horn
Journal:  Arch Dermatol       Date:  1999-03

2.  Localized acquired hypertrichosis following cast application.

Authors:  A Kara; G Kanra; Y Alanay
Journal:  Pediatr Dermatol       Date:  2001 Jan-Feb       Impact factor: 1.588

3.  Hypertrichosis with hereditary gingival hyperplasia.

Authors:  G B Winter; M J Simpkiss
Journal:  Arch Dis Child       Date:  1974-05       Impact factor: 3.791

4.  [Hypertrichosis languinosa universalis].

Authors:  W R Felgenhauer
Journal:  J Genet Hum       Date:  1969-05

5.  Oliver McFarlane syndrome: a 25-year follow-up.

Authors:  J R Sampson; J L Tolmie; J S Cant
Journal:  Am J Med Genet       Date:  1989-10

6.  The hair collar sign: marker for cranial dysraphism.

Authors:  B A Drolet; L Clowry; M K McTigue; N B Esterly
Journal:  Pediatrics       Date:  1995-08       Impact factor: 7.124

7.  Hairy cutaneous malformations of palms and soles. A hereditary condition.

Authors:  C E Jackson; Q C Callies; E A Krull; A Mehregan
Journal:  Arch Dermatol       Date:  1975-09

8.  Familial cervical hypertrichosis with underlying kyphoscoliosis.

Authors:  O M Reed; J R Mellette; J E Fitzpatrick
Journal:  J Am Acad Dermatol       Date:  1989-06       Impact factor: 11.527

Review 9.  Brachmann-de Lange syndrome. 1994 update.

Authors:  B G Kousseff; P Newkirk; A W Root
Journal:  Arch Pediatr Adolesc Med       Date:  1994-07

10.  Prepubertal hypertrichosis: normal or abnormal?

Authors:  J H Barth; J D Wilkinson; R P Dawber
Journal:  Arch Dis Child       Date:  1988-06       Impact factor: 3.791

View more
  1 in total

Review 1.  [Genetic hair diseases. An update].

Authors:  J Frank; P Poblete-Gutiérrez; K Giehl
Journal:  Hautarzt       Date:  2013-11       Impact factor: 0.751

  1 in total

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