Hereditary Hypotrichosis Simplex of the Scalp (HHSS) is a relatively rare form of hereditary alopecia. Herein, we report 2 additional families affected with this disorder.Sudanese Journal of Dermatology Vol. 3(3) 2005: 128-13
Hereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Mar...
Mammalian hair follicle (HF) is a complex structure which consists of several distinct cell layers. ...
Aim: Hypotrichosis simplex (MIM 146520) is a rare form of monogenic hereditary alopecia. Several gen...
Hereditary hypotrichosis simplex of the scalp is an autosomal dominant disorder, characterized by sp...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
Background: Hypotrichosis simplex of the scalp (HSS; MIM 146520) is a rare autosomal dominant form o...
In 1925, Dr Marie Unna described a rare form of hereditary hypotrichosis in a German multigeneration...
Hypotrichosis simplex (HS) with and without woolly hair (WH) comprises a group of rare, monogenic di...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
Harlequin icthyosis (HI) is inherited as autosomal recessive gene. Many cases are sporadic, but othe...
Hereditary alopecias and ectodermal dysplasias are genetically heterogeneous groups of congenital di...
Aim: Hypotrichosis simplex (MIM 146520) is a rare form of monogenic hereditary alopecia. Several gen...
We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a f...
There are several forms of hereditary human hair loss, known collectively as alopecias, which vary i...
AbstractWhile there have been significant advances in understanding the genetic etiology of human ha...
Hereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Mar...
Mammalian hair follicle (HF) is a complex structure which consists of several distinct cell layers. ...
Aim: Hypotrichosis simplex (MIM 146520) is a rare form of monogenic hereditary alopecia. Several gen...
Hereditary hypotrichosis simplex of the scalp is an autosomal dominant disorder, characterized by sp...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
Background: Hypotrichosis simplex of the scalp (HSS; MIM 146520) is a rare autosomal dominant form o...
In 1925, Dr Marie Unna described a rare form of hereditary hypotrichosis in a German multigeneration...
Hypotrichosis simplex (HS) with and without woolly hair (WH) comprises a group of rare, monogenic di...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
Harlequin icthyosis (HI) is inherited as autosomal recessive gene. Many cases are sporadic, but othe...
Hereditary alopecias and ectodermal dysplasias are genetically heterogeneous groups of congenital di...
Aim: Hypotrichosis simplex (MIM 146520) is a rare form of monogenic hereditary alopecia. Several gen...
We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a f...
There are several forms of hereditary human hair loss, known collectively as alopecias, which vary i...
AbstractWhile there have been significant advances in understanding the genetic etiology of human ha...
Hereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Mar...
Mammalian hair follicle (HF) is a complex structure which consists of several distinct cell layers. ...
Aim: Hypotrichosis simplex (MIM 146520) is a rare form of monogenic hereditary alopecia. Several gen...
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