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Ectodermal Dysplasia (ED)
refers to a
group of
genetic disorders characterized by the
abnormal development or
function of two or more
structures that originate...
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wedge in the
ectodermal region.
These special cells are
called medial hinge cells (MHPs). As the
ectoderm continues to elongate, the
ectodermal cells of the...
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Hypohidrotic ectodermal dysplasia is one of
about 150
types of
ectodermal dysplasia in humans.
These disorders result in the
development of structures...
- Ectrodactyly–
ectodermal dysplasia–cleft syndrome, or EEC, and also
referred to as EEC
syndrome and
split hand–split foot–
ectodermal dysplasia–cleft syndrome: 520 ...
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Techanukul T,
Holden ST, et al. (September 2010). "Rapp–Hodgkin and Hay–Wells
ectodermal dysplasia syndromes represent a
variable spectrum of the same genetic...
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Chronic mucocutaneous candidiasis. Hypoparathyroidism. Addison's disease.
Ectodermal dystrophy (skin,
dental enamel, and nails). APS-1 may also cause: Autoimmune...
- Tetra-amelia
syndrome (tetra- + amelia), also
called autosomal recessive tetraamelia, is an
extremely rare
autosomal recessive congenital disorder characterized...
- Clouston's
hidrotic ectodermal dysplasia is a
medical condition caused by
mutations in a
connexin gene, GJB6 or connexin-30,
characterized by
scalp hair...
- The
apical ectodermal ridge (AER) is a
structure that
forms from the
ectodermal cells at the
distal end of each limb bud and acts as a
major signaling...
- include:
Arthrogryposis multiplex due to
muscular dystrophy.
Arthrogryposis ectodermal dysplasia other anomalies, also
known as Cote
Adamopoulos Pantelakis syndrome...
