Hereditary hypotrichosis simplex of the scalp is an autosomal dominant disorder, characterized by sparse or absent scalp hairs without structural defects, in the absence of other ectodermal or systemic abnormalities. Hairs are usually normal at birth but thin progressively during childhood to become very sparse or may be absent by the third decade. Hair loss is confined only to the scalp with normal growth of facial and body hairs
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectoderma...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
AbstractWhile there have been significant advances in understanding the genetic etiology of human ha...
Hereditary Hypotrichosis Simplex of the Scalp (HHSS) is a relatively rare form of hereditary alopeci...
Marie Unna hereditary hypotrichosis has been described in over a dozen families since 1924. Features...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
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...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Hypotrichosis with juvenile macular dystrophy is a rare autosomal recessive disease, characterized b...
This article presents a clinical approach to patchy, non-scarring hair loss and includes conditions ...
Alopecia, a generic term for hair loss, results from a diminution of visible hair and there are seve...
none3Androgenetic alopecia (AGA) is the most common type of hair loss in adults. Although there are ...
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectoderma...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
AbstractWhile there have been significant advances in understanding the genetic etiology of human ha...
Hereditary Hypotrichosis Simplex of the Scalp (HHSS) is a relatively rare form of hereditary alopeci...
Marie Unna hereditary hypotrichosis has been described in over a dozen families since 1924. Features...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
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...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Hypotrichosis with juvenile macular dystrophy is a rare autosomal recessive disease, characterized b...
This article presents a clinical approach to patchy, non-scarring hair loss and includes conditions ...
Alopecia, a generic term for hair loss, results from a diminution of visible hair and there are seve...
none3Androgenetic alopecia (AGA) is the most common type of hair loss in adults. Although there are ...
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectoderma...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
AbstractWhile there have been significant advances in understanding the genetic etiology of human ha...