Results 201 to 210 of about 8,285 (255)

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.
R O, Hess, H, Uno
openaire   +2 more sources

Eyelid cysts, hypodontia, and hypotrichosis

Journal of the American Academy of Dermatology, 1984
We report a case of multiple ectodermal defects with the principal features of eyelid apocrine hydrocystomas , hypodontia, and hypotrichosis. To the best of our knowledge this is the second such report and presents histologic features that are unique in our experience.
J M, Burket, B J, Burket, D A, Burket
openaire   +2 more sources

Recurrent c.459 C>A mutation of the PERP gene results in severe Olmsted syndrome with congenital hypotrichosis, atopic dermatitis, and growth retardation

Journal of dermatology (Print), 2021
Dear Editor, Olmsted syndrome (OS) is a rare genetic condition characterized by bilateral mutilating palmoplantar keratoderma (PPK) and periorificial keratosis.1 Mutations in TRPV3 and MBTPS2 have been reported to account for OS.2,3 Recently, PERP ...
Deyu Song, X. Ran, Yusha Chen, Zhongtao Li, Fan Li, Ying Lan, Sheng Wang   +6 more
semanticscholar   +1 more source

Hypotrichosis in Miniature Poodle Siblings

Journal of the American Veterinary Medical Association, 1975
SUMMARY Progressive hypotrichosis was detected in 2 silver male Miniature Poodle siblings at 5 weeks of age. A male and 2 female siblings had normal black coats. The sire, a 3-year-old black Miniature Poodle, and the dam, a 2-year-old silver Miniature Poodle, also had normal coats.
J D, Conroy, B A, Rasmusen, E, Small
openaire   +2 more sources

Novel small‐insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis

Journal of dermatology (Print), 2020
Autosomal recessive woolly hair/hypotrichosis (ARWH/H) is a rare form of congenital alopecia, which can be caused by mutations in lipase H (LIPH), lysophosphatidic acid receptor 6 (LPAR6/P2RY5) or keratin 25 (KRT25) genes.
H. Lv, Ming Li, R. Cheng
semanticscholar   +1 more source

Marie Unna hereditary hypotrichosis.

European journal of dermatology : EJD, 1999
Hereditary congenital hypotrichosis is an autosomal dominant pilar dysplasia first described by Marie Unna in an extended German family. The diffuse hair defect typically occurs as an isolated phenomenon and the ultrastructural hair findings consist of both torsion and longitudinal grooving of the hair shaft.
G. Argenziano, E. Sammarco, ROSSI, Alfredo, M. Delfino, CALVIERI, Stefano   +4 more
openaire   +3 more sources

Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin

British Journal of Dermatology, 2019
Hypotrichosis simplex of the scalp (HSS) is characterized by progressive loss of scalp hair that results in almost complete baldness at a young age.
A. Peled, L. Samuelov, O. Sarig, R. Bochner, L. Malki, M. Pavlovsky, E. Pichinuk, M. Weil, E. Sprecher   +8 more
semanticscholar   +1 more source

Eyebrow growth pattern analysis in patients with eyebrow hypotrichosis after receiving topical treatment: A retrospective study

Journal of Cosmetic Dermatology, 2020
Differences in growth patterns among the various parts of the eyebrow have been observed.
Poonkiat Suchonwanit, Sasima Thammarucha
semanticscholar   +1 more source

Efficacy and Safety of Bimatoprost 0.01% for the Treatment of Eyebrow Hypotrichosis: A Randomized, Double-Blind, Vehicle-Controlled Study.

Dermatologic Surgery, 2019
BACKGROUND Eyebrow hypotrichosis is an important dermatological problem. However, there is no standard treatment. OBJECTIVE To study the efficacy and safety of bimatoprost 0.01% for the treatment of eyebrow hypotrichosis.
Poonkiat Suchonwanit, Nongsak Chanasumon, Tueboon Sriphojanart   +2 more
semanticscholar   +1 more source

Hereditary hypotrichosis simplex of the scalp

Clinical Genetics, 1987
Hereditary hypotrichosis simplex of the scalp is a rare trait with onset in early childhood. This phenomenon has been reported only once previously, in a Spanish kindred. This communication describes a case in a Jcwish‐Yemenite kindred with 51 affected individuals and confirms autosomal dominant inheritance.
G, Kohn, A, Metzker
openaire   +2 more sources