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Hereditary Hypotrichosis simplex
Dermatology, 1998Hypotrichosis 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 +4 more
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British Journal of Dermatology, 2006
A syndrome of hereditary hypotrichosis with an unusual natural history and clinical features was encountered in a Caucasian family of four generations with a total of twenty-four members of whom eleven were affected. The mode of inheritance was autosomal dominant with variable penetrance.
B, Bentley-Phillips, H J, Grace
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A syndrome of hereditary hypotrichosis with an unusual natural history and clinical features was encountered in a Caucasian family of four generations with a total of twenty-four members of whom eleven were affected. The mode of inheritance was autosomal dominant with variable penetrance.
B, Bentley-Phillips, H J, Grace
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Congenital atrichia and hypotrichosis
World Journal of Pediatrics, 2011Alopecia 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 +2 more
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Hereditary hypotrichosis of the scalp
American Journal of Medical Genetics, 1991AbstractHypotrichosis 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
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Eyelid cysts, hypodontia, and hypotrichosis
Journal of the American Academy of Dermatology, 1984We 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
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Hypotrichosis in Miniature Poodle Siblings
Journal of the American Veterinary Medical Association, 1975SUMMARY 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
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Marie Unna hereditary hypotrichosis.
European journal of dermatology : EJD, 1999Hereditary 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 +4 more
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Hereditary hypotrichosis simplex of the scalp
Clinical Genetics, 1987Hereditary 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
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Hypotrichosis congenita hereditaria Typ M. Unna
Archiv für Dermatologie und Syphilis, 1953Es wird uber weitere Falle der von M. Unna bereits beschriebenen erblichen Hypotrichose bei einer niedersachsischen Familie berichtet. Die Haaranomalie ist klinisch durch hochgradige angeborene Haararmut, verspatet auftretendes Wachstum borstigen Kopfhaares, fruhzeitig einsetzendem, zu fast volliger Kahlheit fuhrendem Haarausfall, histologisch (im ...
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