Ectodermal dysplasia (ED) is a group of genetic
syndromes all deriving from abnormalities of the
ectoderm
The ectoderm is one of the three primary germ layers formed in early embryonic development. It is the outermost layer, and is superficial to the mesoderm (the middle layer) and endoderm (the innermost layer). It emerges and originates from the o ...
al structures.
[James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. .] More than 150 different syndromes have been identified.
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
In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. The first variant is termed dominant and ...
or
recessive
In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. The first variant is termed dominant and ...
.
Ectodermal dysplasias are described as "heritable conditions in which there are abnormalities of two or more ectodermal structures such as the
hair,
teeth
A tooth ( : teeth) is a hard, calcified structure found in the jaws (or mouths) of many vertebrates and used to break down food. Some animals, particularly carnivores and omnivores, also use teeth to help with capturing or wounding prey, te ...
,
nails,
sweat glands,
salivary glands
The salivary glands in mammals are exocrine glands that produce saliva through a system of ducts. Humans have three paired major salivary glands ( parotid, submandibular, and sublingual), as well as hundreds of minor salivary glands. Salivar ...
, cranial-facial structure, digits and other parts of the body."
Presentation
Hair
Individuals affected by an ED syndrome frequently have abnormalities of the hair follicles. Scalp and body hair may be thin, sparse, and very light in color, even though beard growth in affected males may be normal. The hair may grow very slowly or sporadically and it may be excessively fragile, curly, or even twisted. Kinky hair is also a possibility.
Nails
Fingernails and toenails may be thick, abnormally shaped, discolored, ridged, slow-growing, or brittle. The cuticles may be prone to infections.
Skin
The skin may be lightly pigmented. Skin sustaining injury may grow back permanently hypo-pigmented. In some cases, red or brown pigmentation may be present. Skin can be prone to rashes or infections and can be thick over the palms and soles. Care must be taken to prevent cracking, bleeding, and infection.
Sweat glands
Individuals affected by certain ED syndromes cannot
perspire. Their sweat glands may function abnormally or may not have developed at all because of inactive proteins in the sweat glands. Without normal sweat production, the body cannot regulate temperature properly. Therefore, overheating is a common problem, especially during hot weather. Access to cool environments is important.
Salivary glands
Several studies have examined salivary flow rate in individuals and found parotid and submandibular salivary flow ranging from 5 to 15 times lower than average. This is consistent with the salivary glands being of ectodermal origin, although some findings have suggested that there is also mesodermal input.
Teeth
The development of tooth buds frequently results in congenitally absent teeth (in many cases a lack of a permanent set) and/or in the growth of teeth that are peg-shaped or pointed. The enamel may also be defective. Cosmetic dental treatment is almost always necessary and children may need dentures as early as two years of age. Multiple denture replacements are often needed as the child grows, and dental implants may be an option in adolescence, once the jaw is fully grown. Nowadays the option of extracting the teeth and substituting them with dental implants is quite common. In other cases, teeth can be crowned. Orthodontic treatment also may be necessary. Because dental treatment is complex, a multi-disciplinary approach is best.
Other features
People with ED often have certain cranial-facial features which can be distinctive:
frontal bossing is common, longer or more pronounced chins are frequent, broader noses are also very common. Sunken cheeks, wrinkled hyper pigmented periorbital skin , thick everted protuberant lips are also seen in ED cases .In some types of ED, abnormal development of parts of the eye can result in dryness of the eye, cataracts, and vision defects. Professional eye care can help minimize the effects of ED on vision. Similarly, abnormalities in the development of the ear may cause hearing problems. Respiratory infections can be more common because the normal protective secretions of the mouth and nose are not present. Precautions must be taken to limit infections..
Genetics
ED can be classified by inheritance (autosomal dominant, autosomal recessive and
X-linked
Sex linked describes the sex-specific patterns of inheritance and presentation when a gene mutation (allele) is present on a sex chromosome (allosome) rather than a non-sex chromosome ( autosome). In humans, these are termed X-linked recessive, ...
) or by which structures are involved (hair, teeth, nails and/or sweat glands).
There are several different types with distinct genetic causes:
*
Hay–Wells syndrome (
Rapp–Hodgkin syndrome) and
EEC syndrome are all associated with ''
TP63
Tumor protein p63, typically referred to as p63, also known as transformation-related protein 63 is a protein that in humans is encoded by the ''TP63'' (also known as the '' p63'') gene.
The ''TP63'' gene was discovered 20 years after the disco ...
''.
*
Hypohidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia in humans. Before birth, these disorders result in the abnormal development of structures including the skin, hair, nails, teeth, and sweat glands.Freedberg, et ...
can be associated with ''
EDA'', ''
EDAR'' and ''
EDARADD
Ectodysplasin-A receptor-associated adapter protein is a protein that in humans is encoded by the ''EDARADD'' gene.
Function
This gene was identified by its association with ectodermal dysplasia, and specifically with hypohidrotic ectodermal d ...
''.
*
Margarita Island ectodermal dysplasia is associated with ''
PVRL1''.
*
Ectodermal dysplasia with skin fragility is associated with ''
PKP1''.
*
Clouston's hidrotic ectodermal dysplasia is associated with ''
GJB6''.
*
Naegeli syndrome/
Dermatopathia pigmentosa reticulariss is associated with ''
KRT14
Keratin 14 is a member of the type I keratin family of intermediate filament proteins. Keratin 14 was the first type I keratin sequence determined.
Keratin 14 is also known as cytokeratin-14 (CK-14) or keratin-14 (KRT14). In humans it is encoded ...
''.
*
Pachyonychia congenita is caused by multiple keratins.
*
Focal dermal hypoplasia is associated with ''
PORCN''.
*
Ellis–van Creveld syndrome is associated with ''
EVC EVC may refer to:
* Eastern Valley Conference, a defunct American high school athletics conference
* Ecological vegetation class
* Economic value to the customer
* Eden Village Camp, a Jewish summer camp in New York state
* Electric Vehicle Comp ...
''.
*
Palmoplantar ectodermal dysplasia
Palmoplantar ectodermal dysplasia is a cutaneous condition.
Types include:
* Palmoplantar ectodermal dysplasia type 1 or Pachyonychia congenita type I
* Palmoplantar ectodermal dysplasia type 3 or Acrokeratoelastoidosis
* Palmoplantar ectoderm ...
refers to several different conditions selectively affecting the hands and feet.
Diagnosis
In terms of the clinical evaluation, clinical features are the classification method
Treatment
Management for this condition is symptom specific
Society and culture
Notable cases
*
Michael Berryman
Michael John Berryman (born September 4, 1948) is an American character actor. Berryman was born with hypohidrotic ectodermal dysplasia, a rare condition characterized by the absence of sweat glands, hair, and fingernails; his unusual physical ...
, American actor with
hypohidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia in humans. Before birth, these disorders result in the abnormal development of structures including the skin, hair, nails, teeth, and sweat glands.Freedberg, et ...
*
Levi Hawken, New Zealand skateboarder and artist who became well known in 2011 in New Zealand for the "
Nek minnit" viral video on
YouTube
YouTube is a global online video sharing and social media platform headquartered in San Bruno, California. It was launched on February 14, 2005, by Steve Chen, Chad Hurley, and Jawed Karim. It is owned by Google, and is the second most ...
See also
*
List of cutaneous conditions
Many skin conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands. The major function of this system is as a barrier agai ...
*
List of cutaneous conditions caused by mutations in keratins
There are many different keratin proteins normally expressed in the human integumentary system. Mutations in keratin proteins in the skin can cause disease.
Of note, other structural proteins in the epidermis of the skin that are closely rel ...
References
External links
{{Congenital malformations and deformations of integument
Genodermatoses
Syndromes affecting teeth
Ectoderm