Olmsted syndrome with hypotrichosis.
Indian journal of dermatology, venereology and leprology, 2012 Olmsted syndrome is characterised by mutilating palmoplantar keratoderma with peri-orificial hyperkeratosis. We report the case of an 8-year old boy who presented with severe keratoderma of the soles since birth and of the palms from the age of 3 years. At 3 years of age hyperkeratotic plaques appeared on the elbows and knees.
D, Dogra +3 more
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Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3 [PDF]
, 2005 Sen Yang +13 more
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Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats [PDF]
, 2005 Hisham Bazzi +3 more
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Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report [PDF]
, 2021 Giovanna Carnovale-Scalzo +9 more
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The Ultimate Synonym Group [PDF]
, 1987 What is the most talked-about subject in the English-speaking world today? Baldness! How do I know?
Borgmann, Dmitri A.
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Hypotrichosis in a child with olmsted syndrome
Indian Dermatology Online Journal, 2018 Kaliaperumal Karthikeyan +2 more
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A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report. [PDF]
, 2016 Oral-facial-digital syndrome as heterogeneous developmental conditions is characterized by abnormalities in the oral cavity, facial features and digits.
Baple, EL +10 more
core
Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion [PDF]
, 2006 Piranit Nik Kantaputra +5 more
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Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis [PDF]
, 2017 Bíró, Tamás +8 more
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