Focal Facial Dermal Dysplasia 1, Brauer Type (FFDD1)

Alias:

Bitemporal Aplasia Cutis Congenita

Brauer Syndrome

Ffdd1

Hereditary Symmetrical Aplastic Nevi of Temples

Focal Facial Dermal Dysplasia Type I

Focal Facial Dermal Dysplasia Type 1

Focal Facial Dermal Dysplasia

Ffdd Type I

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Focal Facial Dermal Dysplasia 1, Brauer Type, also known as bitemporal aplasia cutis congenita, is related to palmoplantar keratoderma, punctate type ia and focal facial dermal dysplasia 3, setleis type. Affiliated tissues include skin, and related phenotypes are abnormal facial shape and sparse hair

Related ID：

MALACARDS：FCL067

OMIM：136500