Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/20.500.12104/41178
Título: Ehlers-danlos syndrome type VIIC: A Mexican case report
Autor: Rincon-Sanchez, A.R.
Arce, I.E.
Tostado-Rabago, E.A.
Vargas, A.
Padilla-Gomez, L.A.
Bolanos, A.
Barrios-Guyot, S.
Anguiano-Alvarez, V.M.
Ledezma-Rodriguez, V.C.
Islas-Carbajal, M.C.
Rivas-Estilla, A.M.
Feria-Velasco, A.
Davalos, N.O.
Fecha de publicación: 2012
Resumen: Ehlers-Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders whose primary clinical features include soft and extensible skin, articular hypermobility and tissue fragility. EDS type VIIC or 'human dermatosparaxis' is an autosomal recessive disease characterized by severe skin fragility and sagging redundant skin (major criteria) with a soft, doughy texture, easy bruising, premature rupture of fetal membranes and large hernias (minor criteria). Dermatosparaxis (meaning 'tearing of skin'), which has been described in several non-human species, is a disorder of the connective tissue resulting from a deficiency of the enzyme that cleaves the registration peptide off the N-terminal end of collagen after it has been secreted from fibroblasts. We describe a Mexican case from consanguineous parents with all the phenotypical characteristics previously described, plus skeletal abnormalities. Copyright 2012 S. Karger AG, Basel.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-84860730577&partnerID=40&md5=68ebc558d7511a76931082cb0fd73f57
http://hdl.handle.net/20.500.12104/41178
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