-
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...
-
Ectodermal Dysplasia (ED)
refers to a
group of
genetic disorders characterized by the
abnormal development or
function of two or more
structures that originate...
-
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 ...
- one of at
least 150
known types of
ectodermal dysplasia.
These disorders affect tissues that
arise from the
ectodermal germ layer, such as skin, hair, and...
-
Techanukul T,
Holden ST, et al. (September 2010). "Rapp–Hodgkin and Hay–Wells
ectodermal dysplasia syndromes represent a
variable spectrum of the same genetic...
-
Chronic mucocutaneous candidiasis. Hypoparathyroidism. Addison's disease.
Ectodermal dystrophy (skin,
dental enamel, and nails). APS-1 may also cause: Autoimmune...
- Clouston's
hidrotic ectodermal dysplasia is a
medical condition caused by
mutations in a
connexin gene, GJB6 or connexin-30,
characterized by
scalp hair...
- include:
Arthrogryposis multiplex due to
muscular dystrophy.
Arthrogryposis ectodermal dysplasia other anomalies, also
known as Cote
Adamopoulos Pantelakis syndrome...
- Skin
fragility syndrome (also
known as "plakophilin 1 deficiency") is a
cutaneous condition characterized by trauma-induced
blisters and erosions. It is...
