| Demographic Data | 
	| Relation to Proband | 
	proband | 
	| Age at Sampling | 
	3 YR | 
	| Sex | 
	Male | 
	| Age of Onset(If not a control) | 
	21 MO | 
	| Age at Diagnosis(If not a control) | 
	29 MO | 
	| Hispanic or Latino/Not Hispanic or Latino | 
	Not Hispanic/Latino | 
	| Racial Category | 
	Asiatic Indian | 
	| Country | 
	INDIA | 
	|   | 
	| Data Elements | 
	| Clinical Element Type: General NIGMS Catalog Remarks | 
	|    (Baseline)  | 
	| Mutation Information | 
	| Gene, variant, consequence, and exon number: | 
	 GAMT, C.424_426DELGAG, P.GLU142DEL IN EXON 4; SHOWN BY FOCUSED EXOME SEQUENCING | 
	| Zygosity: | 
	 Homozygous Notes: VARIANT INHERITED FROM BOTH MOTHER AND FATHER | 
	| Other variants: | 
	 KCNQ2, C.2323A>G (P.ARG775GLY), HETEROZYGOUS VARIANT OF UNCERTAIN SIGNIFICANCE, INHERITED FROM FATHER; MCM6, C.1366G>A (P.VAL456MET), HETEROZYGOUS VARIANT OF UNCERTAIN SIGNIFICANCE (RS191517067) | 
	| Age of Symptom Onset and Age at Diagnosis | 
	| Age of Symptom Onset: | 
	 21 MONTHS | 
	| Age at Diagnosis: | 
	 29 MONTHS | 
	| In Utero History Information | 
	|   | 
	 | 
	| Birth History Information | 
	|   | 
	 | 
	| Dysmorphic Features | 
	|   | 
	 | 
	| Additional Information: | 
	 PROMINENCE OF NASOPHARYNGEAL ADENOIDS INDENTS THE AIRWAY | 
	| Neurological Symptoms | 
	|   | 
	Sleep abnormalities
  | 
	| Additional Information: | 
	 MRI SCAN REVEALED FOCAL BILATERALLY SYMMETRIC FOCI OF ALTERED SIGNAL & DIFFUSION RESTRICTION INVOLVING THE DORSAL PONS & MEDULLARY TEGMENTUM / CENTRAL TEGMENTAL TRACTS (MEDIAL LONGITUDINAL FASCICULUS); CEREBRAL DYSRHYTHMIA | 
	| Optical and Audiological Symptoms | 
	|   | 
	 | 
	| Additional Information: | 
	 EYE BLINKING | 
	| Musculoskeletal Symptoms | 
	|   | 
	 | 
	| Developmental Milestones | 
	|   | 
	Delayed speech and language development Delayed fine motor skills Delayed gross motor skills
  | 
	| Gastrointestinal Symptoms | 
	|   | 
	 | 
	| Genitourinary Symptoms | 
	|   | 
	 | 
	| Respiratory and Cardiovascular Symptoms | 
	|   | 
	 | 
	| Cognitive and Behavioral Symptoms | 
	|   | 
	 | 
	| Additional Information: | 
	 MULTIPLE EPISODES OF HEAD DROP (5-6 PER DAY) SINCE 1 MONTH; POOR UNDERSTANDING | 
	| Additional Information | 
	| Uncategorized Symptoms: | 
	 LICKS; MAKES ABNORMAL SOUNDS | 
	| Testing Performed  | 
	| Neurological Testing: | 
	 MRI IMAGING; MR SPECTROSCOPY REVEALED SIGNIFICANT REDUCTION IN CREATININE LEVELS; EEG | 
	| Metabolic, Hematologic, and Endocrinologic Testing: | 
	 AMINO ACID PLASMA UHPLC REVEALED NO SIGNIFICANT ABNORMALITY; GUANADINO COMPOUNDS IN PLASMA AND URINE REVEALED LOW LEVELS OF CREATINE AND ELEVATED GAA; URIC ACID SERUM; LFT-A; CALCIUM SERUM; CREATININE SERUM; UREA SERUM; ELECTROLYTES; CBP (COMPLETE BLOOD PICTURE) | 
	| Treatments and Assistive Devices | 
	|   | 
	Occupational therapy Physical therapy Speech therapy
  | 
	| Medications | 
	|   | 
	 SABRIL; TAURINE; CREATINE MONOHYDRATE; METANUTRITION; SODIUM BENZOATE; ORNITHINE; TETRAFOL PLUS; RIVOTRIL; LEVIPIL; NEOPEPTINE; A-Z VITAMIN; ULTRA D3; ASPIRITO; CEFIXIME (FOR STOMACH ILLNESS) | 
	| Family History | 
	| Remarks | 
	See Phenotypic Data tab. |