V-3
Case#: V3, Pakistan, female, 23 years old (report),
DiseaseAssertion: GAMT deficiency
FamilyInfo: Patient V3 is a sister of V1. Consanguineous family.
CasePresentingHPOs: HP:0010864, HP:0001250, HP:0001257, HP:0003487, HP:0001251, HP:0001761 (severe intellectual disability, seizure, spasticity, Babinski sign, ataxia, pes cavus)
CaseHPOFreeText: Neonatal onset of seizures, Spasticity in upper and lower limbs, Peripheral neuropathy probably present, sitting delayed, standing delayed, walking delayed, never developed speech
CaseNotHPOs: HP:0001347 (hyperreflexia)
CaseNotHPOFreeText: Bed ridden, recurrent bone fractures
Biochemical analyte testing:
Brain Magnetic Resonance Spectroscopy (MRS): N/A
GAMT activity assay: N/A
Zygosity: Homozygous / compound heterozygous.
Variant 1: c.134G > A (p.Trp45)
ClinVarID: N/A
CAID: N/A
gnomAD: N/A
Variant 2: N/A
ClinVarID: N/A
CAID: N/A
gnomAD: N/A
ParentalGenotypes: Both parents confirmed to be heterozygous for c.134G > A
AlsoPublished: N/A