Phenotypes for disease #01301 (EDSHMB (Ehlers-Danlos syndrome, hypermobility type (EDSHMB, EDS3)), OMIM:130020)

3 entries on 1 page. Showing entries 1 - 3.
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0000106398 hypertelorism, pectus excavatum, clubfeet translucent skin, bilateral inguinal hernia and hypermobile joints muscle hypotonia poor muscle mass hydro-ureteronephrosis, hypospadias, food allergies, chronic diarrhea, recurrent bronchitis elongated cusps of the tricuspid valve with regurgitation thinned and elongated cusps of the mitral valve with mitral valve prolapse dilation of the pulmonary arteries with pulmonary hypertension and atrial septum defect with right atrial and ventricular dilatation broader interhemispheric fissures and subarachnoid spaces with echogenic parenchyma died due to severe pulmonary hypertension and heart failure - - Familial, autosomal dominant - - - - - Elyssa Cannaerts 00133648
0000303488 Recurrent joint dislocations and chronic widespread pain. Skin was fragile, hyperextensible and had a soft and doughy aspect with remarkable translucency.reported severe bruising tendency, and varicose veins at a young age. She presented generalised joint hypermobility of both distal and proximal joints with a Beighton score of 7/9. hEDS - Familial 49y - - - - Oumaima Nehaili 00411451
0000337700 - Hypermobile EDS Hypermobile EDS Familial, autosomal dominant - 19y 14y - - Katelyn Schneider 00448523
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