Pathologic Condition

Ectodermal Dysplasia

AMW:DIS:160009

A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.

Pathology clinical

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Ectodermal Dysplasia has parent Abnormalities, Multiple

Focal Dermal Hypoplasia has parent Ectodermal Dysplasia

Ellis-Van Creveld Syndrome has parent Ectodermal Dysplasia

Neurocutaneous Syndromes has parent Ectodermal Dysplasia

Ectodermal Dysplasia 1, Anhidrotic has parent Ectodermal Dysplasia

Ectodermal Dysplasia 3, Anhidrotic has parent Ectodermal Dysplasia

Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive has parent Ectodermal Dysplasia

Focal Facial Dermal Dysplasias has parent Ectodermal Dysplasia

Pachyonychia Congenita has parent Ectodermal Dysplasia

Ectodermal Dysplasia has parent Skin Abnormalities

Ectodermal Dysplasia has parent Skin Diseases, Genetic

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