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Diffuse congenital hypotrichosis simplex with associated hair shaft fragility

Autor: Rodney Sinclair, Anneliese Willems

Publikováno v: The Australasian journal of dermatologyREFERENCES. 63(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f93c4f355b32b0f16a8932283d63538
https://pubmed.ncbi.nlm.nih.gov/34657286

A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle

Autor: Jacinto, Joana G. P., Markey, Alysta D., Veiga, Inês M. B., Paris, Julia M., Welle, Monika, Beever, Jonathan E., Drögemüller, Cord

Publikováno v: Genes
Volume 12
Issue 7
Genes, Vol 12, Iss 1038, p 1038 (2021)
Jacinto, Joana G. P.; Markey, Alysta D.; Veiga, Inês M. B.; Paris, Julia M.; Welle, Monika; Beever, Jonathan E.; Drögemüller, Cord (2021). A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle. Genes, 12(7), p. 1038. MDPI, Molecular Diversity Preservation International 10.3390/genes12071038

Genodermatoses, such as heritable skin disorders, mostly represent Mendelian conditions. Congenital hypotrichosis (HY) characterize a condition of being born with less hair than normal. The purpose of this study was to characterize the clinicopatholo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed65d383d583c6d8fa23250d20ad93c7
http://europepmc.org/articles/PMC8304205

Congenital Hypotrichosis Simplex: A Case Report

Autor: Mohammed Mahbubul Islam, Maria Kibtiar, Shahana A Rahman, Romana Akther

Publikováno v: Bangladesh Journal of Child Health. 43:59-61

Congenital hypotrichosis simplex of scalp is a rare disorder which only affect the scalp hair. Rest of the hair bearing areas are spared. In this disorder the scalp hair are absent or sparse. We describe a 5 month old boy presented with no growth of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::53a5cde6ff56d4c1e948bb4df263ae6d
https://doi.org/10.3329/bjch.v43i1.41219

The hairless (hr) gene is involved in the congenital hypotrichosis of Valle del Belice sheep

Autor: Finocchiaro Raffaella, Portolano Baldassare, Damiani Giuseppe, Caroli Anna, Budelli Elena, Bolla Patrizia, Pagnacco Giulio

Publikováno v: Genetics Selection Evolution, Vol 35, Iss Suppl 1, Pp S147-S156 (2003)

Abstract Congenital hypotrichosis in mammalian species consists of partial or complete absence of hair at birth. The hairless gene is often responsible for this disorder in men, mice and rats. Recent experimental data on Valle del Belice sheep reared

Externí odkaz: https://doaj.org/article/689a4069c09248cab99de8c2f30167f5