Ectodermal dysplasia

Ectodermal dysplasia
A patient displaying peg-shaped teeth and sparse hair characteristic of ectodermal dysplasia.
Specialty	Medical genetics

Ectodermal Dysplasia (ED) refers to a group of genetic disorders characterized by the abnormal development or function of two or more structures that originate from the ectoderm, the outer layer of an embryo. These structures include hair, teeth, nails, and sweat glands, all of which may develop abnormally in people with ED.^[1][2] There are over 200 different syndromes classified under ED, each with a range of symptoms and genetic causes.^[3] The most common type is Hypohidrotic Ectodermal Dysplasia (HED), which affects approximately 1 in every 5,000 to 10,000 live births. HED primarily affects males because it is typically inherited through the X chromosome.^[2][3]

The genetic cause of ED lies in mutations, or changes, in certain genes that play an essential role in forming ectodermal structures. These genes are part of signalling pathways—most notably, the EDA/NF-kappaB pathway—which guide the development of hair, skin, nails, teeth, and glands during embryonic growth. Genes such as EDA, EDAR, and EDARADD are key players in this process, and variants in these genes disrupt normal development, resulting in the characteristic symptoms of ED.^[2][4] Beyond HED, other types of ED follow different inheritance patterns, such as autosomal dominant or autosomal recessive, but often show similar physical traits, though with different genetic mutations.

Diagnosing ED usually involves a clinical examination focused on core symptoms, such as lack of sweating, specific dental and hair abnormalities, and characteristic facial features. Genetic testing can confirm the diagnosis, especially when there is a family history of ED or when prenatal screening is considered.^[1]