Literature DB >> 7537130

Trichorhinophalangeal syndrome.

R Böni1, R H Böni, D Tsambaos, M A Spycher, R M Trüeb.   

Abstract

Trichorhinophalangeal syndrome (TRPS) comprises a distinctive combination of hair, facial and bony abnormalities with variable expression. A 20-year-old man with TRPS was seen because of marked androgenetic alopecia. Scanning electron-microscopic studies of the hair revealed flattened hair with an elliptoid transverse section pattern. Mechanical behavior of the hair was abnormal with a significant increase in the viscous parameter, indicating a decreased intermolecular bridging within the keratin matrix. The dermatologist confronted with premature or marked alopecia in young adults should always consider the possibility of an underlying congenital syndrome involving the hair and prompt further investigation.

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Year:  1995        PMID: 7537130     DOI: 10.1159/000246667

Source DB:  PubMed          Journal:  Dermatology        ISSN: 1018-8665            Impact factor:   5.366


  3 in total

Review 1.  Congenital atrichia and hypotrichosis.

Authors:  Antoni Bennàssar; Juan Ferrando; Ramon Grimalt
Journal:  World J Pediatr       Date:  2011-05-15       Impact factor: 2.764

2.  Severe brachydactyly and short stature resulting from a novel pathogenic TRPS1 variant within the GATA DNA-binding domain.

Authors:  Anara Karaca; Monica Reyes; Lauren T Shumate; Isilay Taskaldiran; Tulay Omma; Nese Ersoz Gulcelik; Murat Bastepe
Journal:  Bone       Date:  2019-03-23       Impact factor: 4.398

3.  Novel Frameshift Mutation in TRPS1 in a Ukrainian Patient with Trichorhinophalangeal Syndrome Type I.

Authors:  Yuliya Ovcharenko; Yuval Ramot
Journal:  Int J Trichology       Date:  2013-07
  3 in total

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