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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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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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Neonatal ichthyosis and hypotrichosis
Pediatric Dermatology, 2019Pedro Vilas Boas +3 more
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Congenital hereditary hypotrichosis(Marie Unna hypotrichosis). Report of two cases
1980We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a family in which the disease appeared in seven members in a period of four generations. We point out the more frequent features of this syndrome: male pattern alopecia, rare hairs resembling a 'horse hair', and follicular atrophy.
S.Menni, C.Crosti
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Hypotrichosis, milia, brachydactyly, and frenula
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2015Antonia, Jeskowiak +2 more
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