Ehlers-Danlos syndrome, dermatosparaxis type: A genetic disorder characterized by extremely fragile and sagging skin caused by mutation in the ADAMTS2 gene.
Dermatosparaxis type (formerly called type VII C)
This form is also very rare. Only about 10 cases have been reported worldwide. Signs and symptoms include: ...
Dermatosparaxis type
(formerly type VIIC)
Patients have severely fragile skin that is soft and doughy with sagging and folding. This rare form of Ehlers-Danlos syndrome can be diagnosed with a skin biopsy.
Tenascin-X deficient type ...
Dermatosparaxis type (VIIC)
the most rare of all six types, with only 10 cases reported worldwide
What causes Ehlers Danlos syndrome?
The dermatosparaxis and kyphoscoliosis types of Ehlers-Danlos syndrome, and some cases of the classic and hypermobility forms, are inherited in an autosomal recessive pattern.
Ehlers-Danlos syndrome, dermatosparaxis type ... joint dislocations
Ehlers-Danlos syndrome, dermatospraxis type ... joint dislocations
Ehlers-Danlos Syndrome, Dysfibronectinemic type ... loose joints
Ehlers-Danlos syndrome, hypermobile type ...
Dermatosparaxis Type Ehlers-Danlos syndrome see Ehlers-Danlos syndrome
Developmental Coordination Disorder see Dyspraxia
Developmental Delay see Global Developmental Delay ...
Ehlers Danlos syndrome, kyphoscoliotic type
Ehlers Danlos syndrome, arthrochalasia type
Ehlers Danlos syndrome, dermatosparaxis type
Ehlers Danlos syndrome, progeroid form
Ehlers Danlos syndrome, cardiac valvular form ...
Efudex Egaten EGD Ege Universitesi Tip Fakultesi Dogumevi Ege Universitesi Tip Fakultesi Hastanesi EGF Egg Egg donation Egg sac Eghbal Ego Ego dystonic Ego ideal Ehlers Danlos Syndrome Ehlers-Danlos syndrome Ehlers-Danlos syndrome, dermatosparaxis ...
 See also: Ehlers-Danlos syndrome, Symptom, Hypermobility, Psoriasis, Arthritis
  
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