Demographic Data |
Relation to Proband |
mother |
Age at Sampling |
38 YR |
Sex |
Female |
Hispanic or Latino/Not Hispanic or Latino |
Not Hispanic/Latino |
Racial Category |
White |
Country |
USA |
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Data Elements |
Clinical Element Type: General NIGMS Catalog Remarks |
(Baseline) |
Mutation Information |
Gene, variant, consequence, and exon number: |
SANGER SEQUENCING REVEALED THIS INDIVIDUAL IS HETEROZYGOUS FOR THE C.1475T>C (P.L492P) IN EXON 11 OF THE SLC13A5 GENE |
Zygosity: |
Heterozygous Notes: CLINICALLY UNAFFECTED MOTHER OF 2 AFFECTED CHILDREN; BOTH CHILDREN (GM27288 & GM27289) ARE COMPOUND HETEROZYGOUS FOR TWO VARIANTS IN THE SLC13A5 GENE: SLC13A5 C.655G>A (P.G219R) EXON 5; SLC13A5 C.1475T>C (P.L492P) EXON 11 |
Age of Symptom Onset and Age at Diagnosis |
In Utero History Information |
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Birth History Information |
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Dysmorphic Features |
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Neurological Symptoms |
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Optical and Audiological Symptoms |
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Musculoskeletal Symptoms |
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Developmental Milestones |
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Gastrointestinal Symptoms |
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Genitourinary Symptoms |
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Respiratory and Cardiovascular Symptoms |
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Cognitive and Behavioral Symptoms |
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Additional Information |
Testing Performed |
Treatments and Assistive Devices |
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Medications |
Family History |