Group of genetic conditions affecting the embryonic ectoderm
Medical condition
Ectodermal dysplasia
A patient displaying peg-shaped teeth and sparse hair characteristic of ectodermal dysplasia.
Specialty
Medical genetics
Ectodermal dysplasia (ED) is a group of genetic syndromes all deriving from abnormalities of the ectodermal structures.[1]: 570 More than 150 different syndromes have been identified.[2]
Despite some of the syndromes having different genetic causes, the symptoms are sometimes very similar. Diagnosis is usually by clinical observation, often with the assistance of family medical histories so that it can be determined whether transmission is autosomal dominant or recessive.
Ectodermal dysplasias are described as "heritable conditions in which there are abnormalities of two or more ectodermal structures such as the hair, teeth, nails, sweat glands, salivary glands, cranial-facial structure, digits and other parts of the body."[citation needed]
^James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
^Pinheiro M, Freire-Maia N (November 1994). "Ectodermal dysplasias: a clinical classification and a causal review". Am. J. Med. Genet. 53 (2): 153–62. doi:10.1002/ajmg.1320530207. PMID 7856640.
and 21 Related for: Ectodermal dysplasia information
Hypohidrotic ectodermaldysplasia is one of about 150 types of ectodermaldysplasia in humans. Before birth, these disorders result in the abnormal development...
of the mutations involved with an ectodermaldysplasia subtype have been identified. Hypohidrotic ectodermaldysplasia (HED) is the most common subtype...
only medical condition) or comorbid with other syndromes, such as ectodermaldysplasia, Syndactyly (Poland's syndrome) and lipoatrophic diabetes. This abnormality...
Arthrogryposis multiplex due to muscular dystrophy. Arthrogryposis ectodermaldysplasia other anomalies, also known as Cote Adamopoulos Pantelakis syndrome...
Hypohidrotic/anhidrotic ectodermaldysplasia with immune deficiency is a rare genetic condition characterized by a combination of the features of ectodermaldysplasia alongside...
infections.: 502 This is an Autosomal recessive variant of ectodermaldysplasia.: 502 EctodermalDysplasia has a rare incidence estimated between 1/10,000 – 1/100...
Palmoplantar ectodermaldysplasia is a cutaneous condition. Types include:[citation needed] Palmoplantar ectodermaldysplasia type 1 or Pachyonychia congenita...
Ectodermaldysplasia with corkscrew hairs is a skin condition with salient features including exaggerated pili torti, scalp keloids, follicular plugging...
the hair cells, and the sweat glands. It is a type of syndromic ectodermaldysplasia. Individuals with this condition typically have the following symptoms:...
an American character actor. Berryman was born with hypohidrotic ectodermaldysplasia, a rare condition characterized by the absence of sweat glands, hair...
devout Christian. In 2017, Williams revealed that he was born with ectodermaldysplasia, a rare genetic disorder that caused him to lack a full set of teeth...
Skin fragility syndrome (also known as "plakophilin 1 deficiency") is a cutaneous condition characterized by trauma-induced blisters and erosions. It is...
syndrome (ectrodactyly–ectodermaldysplasia–cleft syndrome). The p63 gene plays a critical role in the development of the apical ectodermal ridge (AER), this...
malformation of the fourth and fifth fingers. It is considered a kind of ectodermaldysplasia. People with ODD syndrome often have a characteristic appearance...
cause ectodermaldysplasia, which is also known as X-linked hypohidrotic ectodermaldysplasia. Common dental features of ectodermaldysplasia are multiple...
associated with the group of skin and nerve syndromes called the ectodermaldysplasias. Anodontia is usually part of a syndrome and seldom occurs as an...