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Results: 3

1.

Scapuloperoneal myopathy

MedGen UID:
419759
Concept ID:
C2931268
Disease or Syndrome
2.

Scapuloperoneal syndrome, neurogenic, Kaeser type

MedGen UID:
356670
Concept ID:
C1867005
Disease or Syndrome
3.

Emery-Dreifuss muscular dystrophy 1, X-linked

Emery-Dreifuss muscular dystrophy (EDMD) is characterized by the clinical triad of joint contractures that begin in early childhood, slowly progressive muscle weakness and wasting initially in a humero-peroneal distribution that later extends to the scapular and pelvic girdle muscles, and cardiac involvement that may manifest as palpitations, presyncope and syncope, poor exercise tolerance, and congestive heart failure. Age of onset, severity, and progression of muscle and cardiac involvement demonstrate both inter- and intrafamilial variability. Clinical variability ranges from early onset with severe presentation in childhood to late onset with slow progression in adulthood. In general, joint contractures appear during the first two decades, followed by muscle weakness and wasting. Cardiac involvement usually occurs after the second decade. [from GeneReviews]

MedGen UID:
148284
Concept ID:
C0751337
Disease or Syndrome

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