We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectodermal dysplasia, subtotal amelia, scoliosis and left renal agenesis. Two other family members had the full clinical criteria of hypohidrotic ectodermal dysplasia, characterized by deficient sweat glands, hypodontia, hypoplasia of the mucous glands, and fine hair. Nine family subjects had variable clinical expression of the disorder. Keywords: Hypohidrotic ectodermal dysplasia (H E D), subtotal amelia, dysplastic ears African Health Sciences Vol. 5 (3) 2005: pp. 270-27
Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-li...
Ectodermal Dysplasia is a disorder that occurs due to abnormal development of at least two major ect...
ABSTRACT Background and Setting: Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenita...
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectoderm...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Autosomal recessive hereditary ectodermal dysplasia (HED) has not been described in sub‑Saharan Afri...
Ectodermal dysplasia (ED) is a inherited genetic disorder with manifestations of abnormalities in mo...
Background: Hypohidrotic Ectodermal Dysplasia (HED) is a genetic disorder which affects structures o...
SummaryA crucial issue in genetic counseling is the recognition of nonallelic genetic heterogeneity....
Background X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by pathogenic variants of...
Ectodermal dysplasia (ED) is a rare hereditary disorder involving two or more of the ectodermal stru...
Ectodermal dysplasias (EDs) are a large group of heritable complex conditions with more than 200 mem...
Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenital syndrome characterized by spars...
We report a 3 month old female, third in order of birth of non consanguineous Egyptian parents with ...
We describe the findings of anhidrotic/hypohidrotic ecto-dermal dysplasia in three successive genera...
Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-li...
Ectodermal Dysplasia is a disorder that occurs due to abnormal development of at least two major ect...
ABSTRACT Background and Setting: Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenita...
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectoderm...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Autosomal recessive hereditary ectodermal dysplasia (HED) has not been described in sub‑Saharan Afri...
Ectodermal dysplasia (ED) is a inherited genetic disorder with manifestations of abnormalities in mo...
Background: Hypohidrotic Ectodermal Dysplasia (HED) is a genetic disorder which affects structures o...
SummaryA crucial issue in genetic counseling is the recognition of nonallelic genetic heterogeneity....
Background X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by pathogenic variants of...
Ectodermal dysplasia (ED) is a rare hereditary disorder involving two or more of the ectodermal stru...
Ectodermal dysplasias (EDs) are a large group of heritable complex conditions with more than 200 mem...
Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenital syndrome characterized by spars...
We report a 3 month old female, third in order of birth of non consanguineous Egyptian parents with ...
We describe the findings of anhidrotic/hypohidrotic ecto-dermal dysplasia in three successive genera...
Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-li...
Ectodermal Dysplasia is a disorder that occurs due to abnormal development of at least two major ect...
ABSTRACT Background and Setting: Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenita...