3 years and 1
Case#: 3 y.o, male, Palestinian-American
DiseaseAssertion: Limb Girdle muscular dystrophy
FamilyInfo: Parents are first cousins. Other two siblings had normal neurologic examination and normal creatine kinase values.
CasePresentingHPOs: HP:0003707, HP:0003701,HP:0003560, HP:0006785, HP:0003236,HP:0003325, HP:0008981, HP:0002515,
CaseHPOFreeText: Bulk was reduced in his shoulder and hip girdle. Bilateral pseudohypertrophy of the calves.
CaseNotHPOs:
CaseNotHPOFreeText:
MotorAchievement: Had a motor delay. Was able to walk well but cant run lifting his knees. Can jump but fell afterwards. Can not raise from without the use of a chair or another person. Walking gait is normal. When he does try to run there is a waddle.
CreatineKinase: 12,323 U/L
CasePreviousTesting:General examination and cranial nerve examination were normal
GenotypingMethod:
PreviouslyPublished:
Variant: NM_000231.2:c.525delT
ClinVar: 189243