Results 211 to 220 of about 5,711 (254)
Some of the next articles are maybe not open access.
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.
Bradley J. Burket +2 more
openaire +3 more sources
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.
H J Grace, B Bentley-Phillips
openaire +3 more sources
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.
H J Grace, B Bentley-Phillips
openaire +3 more sources
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, Aryeh Metzker
openaire +3 more sources
Hereditary Hypotrichosis simplex of the Scalp
Dermatology, 1995We report on a female aged 13 years, whose scalp hair began to disappear at the age of 9 years, leaving only sparse wispy hairs in the parietal-occipital region. Eyelashes, eyebrows and body hair were unaffected. There were no signs of ectodermal dysplasia on the skin, nails, teeth and eyes nor other congenital abnormalities. The family pedigree showed
M. Armijo +3 more
openaire +3 more sources
Congenital hypotrichosis due to short anagen
British Journal of Dermatology, 2000Two children with congenital hypotrichosis are described. Both presented with persistent short, fine hair since birth. Evidence is provided that the short hair observed in these patients is due to a short anagen phase of the hair cycle, with a normal rate of hair growth.
R.M. Trüeb, M.M. Barraud‐Klenovsek
openaire +3 more sources
Hereditary Hypotrichosis Simplex of the Scalp
Pediatric Dermatology, 2002Hereditary hypotrichosis simplex of the scalp is a genotrichosis characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. We describe two Spanish families with hypotrichosis of the scalp.
Aurora Guerra Tapia +3 more
openaire +3 more sources
Marie Unna Hypotrichosis in a Chinese Family [PDF]
Pediatric Dermatology, 2002 Abstract: Marie Unna hypotrichosis is a rare, autosomal dominant hypotrichosis characterized by sparse or absent hair at birth with regrowth of coarse, wiry hair from childhood, followed by progressive loss on approaching puberty. We report a Chinese mother and child seen at our skin center with features of Marie Unna hypotrichosis. The family pedigree
Wong, S.N., Giam, Y.C., Lee, Y.S.
openaire +2 more sources
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
openaire +2 more sources
Congenital hypotrichosis in a Simmental cross heifer
Veterinary Dermatology, 2019BackgroundCongenital hypotrichosis is defined as a less than normal amount of hair, obvious at birth or in the first weeks of life. Causes are nongenetic or genetic.ObjectivesTo describe the clinical presentation and histological features of a novel form of hypotrichosis in a heifer.AnimalA 15‐month‐old Simmental cross‐bred heifer was presented with a ...
Jože Starič +3 more
openaire +3 more sources
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
openaire +3 more sources