Results 201 to 210 of about 5,711 (254)

Hypopigmented Burn Scar Successfully Repigmented With Noninvasive Topical Bimatoprost Treatment. [PDF]

Cureus
Slater KN, Kashlan R, Potts G.
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Hypotrichosis and Juvenile Macular Dystrophy-First Homozygous Family Case from Türkiye

Nazlı Caf, Alper Gezdirici, Murat Karapapak, Erişcan Melih Kırsoy, Elif Çetinkaya, HH Yılmaz, Zafer Türkoğlu   +6 more
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Spatial variation and associated genes of total hair follicle density in goats. [PDF]

Anim Biosci
Zhang J, Chen Z, Zhang S, Li G, Fang X, Zhao Y.   +5 more
europepmc   +1 more source

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Hereditary Hypotrichosis simplex

Dermatology, 1998
Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is especially uncommon. We present a Spanish family with 8 of 19 persons covering 4 generations affected by HHS. No associated ectodermal or other defects were noted.
M. Just, Isabel Bielsa, Carlos Ferrándiz, M.J. Fuente, Miquel Ribera   +4 more
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Hereditary hypotrichosis of the scalp

American Journal of Medical Genetics, 1991
AbstractHypotrichosis of the scalp was found in 4 individuals of a 6‐generation Caucasian family. This congenital phenomenon is a rather rare subtype of hereditary hypotrichosis and affects only scalp hair. The hairs of the scalp were generally sparse and short vellus type from childhood and thinned progressively with age.
Russell O. Hess, Hideo Uno
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Congenital atrichia and hypotrichosis

World Journal of Pediatrics, 2011
Alopecia present from birth includes a broad differential diagnosis and often represents a diagnostic and therapeutic challenge for the involved physician.An initial correct diagnosis and classification is essential because structural hair defects may be the expression of a genetic disorder affecting hair growth, part of a congenital syndrome with ...
Antoni Bennàssar, Juan Ferrando, Ramon Grimalt   +2 more
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Hereditary hypotrichosis simplex: report of a family

Clinical and Experimental Dermatology, 2002
We report a family with hereditary hypotrichosis simplex of the scalp, a rare disorder that was first described in 1974. In our family, four out of 10 siblings were affected, including three females and one male. Examination showed thinning of the scalp hair and sparse body hair. Eyebrows, eyelashes, pubic and axillary hair were normal. Skin, nails and
D. Al Aboud, K. Al Hawsawi, A. Al Githami, K. Al Aboud   +3 more
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