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Ehlers-Danlos syndrome	Ehlers-Danlos syndrome is a group of inherited disorders that affect connective tissue, the tissue that binds and supports the body's muscles, ligaments, organs, and skin. The dermatosparaxis type is characterized by extremely fragile and sagging skin. This form of Ehlers-Danlos syndrome was formerly called type VIIC. Ehlers-Danlos syndrome, dermatosparaxis type is a subtype of Ehlers-Danlos syndrome. ... 출처: goldbamboo.com/glossary-1e.html
Ehlers-Danlos s.	1. a group of inherited disorders of the connective tissue, occurring in at least ten types, I to X, based on clinical, genetic, and biochemical evidence, varying in severity from mild to lethal, and transmitted genetically as autosomal recessive, autosomal dominant, or X-linked recessive traits. The major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors; variably present in some types are cardiovascular, gastrointestinal, orthopedic, and ocular defects. The biochemical defects are known for several types. Type IV, with prominent vascular manifestations, is caused by defects in the structure, synthesis, or secretion of one type of procollagen; type VI, with prominent ocular manifestations, is caused by a deficiency of lysyl hydroxylase; type VII, with multiple joint dislocations, is called also arthrochalasis multiplex congenita and is caused by mutations involving the normal cleavage sites of some procollagen chains; type IX is X-linked cutis laxa; and type X is due to a defect in fibronectin that interferes with normal platelet aggregation. See accompanying illustration. 2. cutaneous asthenia (def. 1). 출처: www.mercksource.com/pp/us/cns/cns_health_library.j...

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome is a group of inherited disorders that affect connective tissue, the tissue that binds and supports the body's muscles, ligaments, organs, and skin. The dermatosparaxis type is characterized by extremely fragile and sagging skin. This form of Ehlers-Danlos syndrome was formerly called type VIIC. Ehlers-Danlos syndrome, dermatosparaxis type is a subtype of Ehlers-Danlos syndrome. ...

출처: goldbamboo.com/glossary-1e.html

Ehlers-Danlos s.

1. a group of inherited disorders of the connective tissue, occurring in at least ten types, I to X, based on clinical, genetic, and biochemical evidence, varying in severity from mild to lethal, and transmitted genetically as autosomal recessive, autosomal dominant, or X-linked recessive traits. The major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors; variably present in some types are cardiovascular, gastrointestinal, orthopedic, and ocular defects. The biochemical defects are known for several types. Type IV, with prominent vascular manifestations, is caused by defects in the structure, synthesis, or secretion of one type of procollagen; type VI, with prominent ocular manifestations, is caused by a deficiency of lysyl hydroxylase; type VII, with multiple joint dislocations, is called also arthrochalasis multiplex congenita and is caused by mutations involving the normal cleavage sites of some procollagen chains; type IX is X-linked cutis laxa; and type X is due to a defect in fibronectin that interferes with normal platelet aggregation. See accompanying illustration. 2. cutaneous asthenia (def. 1).

출처: www.mercksource.com/pp/us/cns/cns_health_library.j...