- Jan 2023
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www.proquest.com www.proquest.com
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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
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girl was 10 years and 11 months
PMID: 11261449
Gene: SGCG
HGNC: 10809
Case#: 10 y.o female, 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:During the physical examination the girl looked alert and aware. Calves were pseudohypertrophy
CaseNotHPOs:
CaseNotHPOFreeText:
MotorAchievement: Learned to walk at 15 months but if she fell couldnt get up. Not able to run by lifting her knees. She fatigued easier than her peers. Can’t stand on one foot. Waddling gait
CreatineKinase: 8,129 U/L
CasePreviousTesting: General examination and cranial nerve examination were normal.
GenotypingMethod: Muscle Biopsy of the quadricep. Immunostaining for sarcoglycan showed particle deficiency. Dystrophin and merson staining were normal
PreviouslyPublished:
Variant: NM_000231.2:c.525delT
ClinVar: 189243
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- Jan 2020
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www.sciencedirect.com www.sciencedirect.com
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axial muscle weakness
Monarch lookup result: https://monarchinitiative.org/phenotype/HP:0003327
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www.sciencedirect.com www.sciencedirect.com
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Gowers’ sign
Monarch lookup result: https://monarchinitiative.org/phenotype/HP:0003391
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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Blood
Monarch lookup result: https://monarchinitiative.org/phenotype/HP:0410211
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fiber degeneration
Monarch lookup result: https://monarchinitiative.org/phenotype/HP:0100295
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SGCG
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