Add to ORKGHereditary 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. A large pedigree comprising 6 generations with 20 members affected by Marie Unna hypotrichosis from Italy is reported
Hereditary hypohidrotic ectodermal dysplasia, also called the Christ-Siemens-Touraine Syndrome is ch...
BackgroundMarie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant disorder characterised...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
Hereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Mar...
We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a f...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
In 1925, Dr Marie Unna described a rare form of hereditary hypotrichosis in a German multigeneration...
Marie Unna hereditary hypotrichosis has been described in over a dozen families since 1924. Features...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant disorder characterized by co...
Marie-Unna hypotrichosis (MU) is a rare autosomal dominant congenital alopecia characterised by prog...
Marie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant form of non-syndromic hereditary...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
SummaryHypotrichosis of Marie Unna (MU) is an autosomal dominant hair-loss disorder with onset in ch...
Hereditary hypohidrotic ectodermal dysplasia, also called the Christ-Siemens-Touraine Syndrome is ch...
BackgroundMarie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant disorder characterised...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
Hereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Mar...
We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a f...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
In 1925, Dr Marie Unna described a rare form of hereditary hypotrichosis in a German multigeneration...
Marie Unna hereditary hypotrichosis has been described in over a dozen families since 1924. Features...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
We report a family with Marie Unna hereditary hypotrichosis (MUHH) from Turkey. MUHH is a distinct f...
Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant disorder characterized by co...
Marie-Unna hypotrichosis (MU) is a rare autosomal dominant congenital alopecia characterised by prog...
Marie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant form of non-syndromic hereditary...
We report on a three-generation Italian family with dominant transmission of a form of hereditary hy...
SummaryHypotrichosis of Marie Unna (MU) is an autosomal dominant hair-loss disorder with onset in ch...
Hereditary hypohidrotic ectodermal dysplasia, also called the Christ-Siemens-Touraine Syndrome is ch...
BackgroundMarie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant disorder characterised...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...