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. 2018 Jan 22;39(4):537–549. doi: 10.1002/humu.23396

Table 1.

Summary of patient clinical features

Subject 1 Subject 2
ISCA2 variant (NM_194279.2) c.229G>A p.Gly77Ser c.229G>A p.Gly77Ser
Gender Male Female
Age of onset 3 m 6 m
Current age 3 y 5 m Deceased
Age at last clinic visit 1 y 9 m 9 m
Age at death N/A 9 m
Growth
Poor growth + +
Poor weight gain +
Head circumference 50th centile Relative macrocephaly
Ophthalmologic
Optic nerve pallor + +
Visual impairment + +
Dysmorphic features
Low set ears +
Broad nasal bridge +
Respiratory
Frequent infections
Tracheostomy
Gastrointestinal
Feeding difficulties/aspiration +/− +/+
Constipation +
Nasogastric tube +
Skeletal
Joint laxity +
Short fourth metacarpals +
Cutaneous toe syndactyly +
Neurological
Development delays + +
Developmental regression +, 6 m +, 6 m
Expressive language
Hypotonia +, truncal +, truncal
Spasticity + +
Abnormal movements
Ambulation
Seizure
Radiological
Leukodystrophy + +
MRS Elevated lactate peak Elevated lactate peak
T1/T2 signal abnormalities Increased T2 in WM of SUF, PVWM extending into PLIC, PB, and SP of CC and CP. Diffuse T1 and T2 in WM of FP, OC, and both CBH
Abnormal signal DTT, ICP, and CWM
Abnormal T2 in CCJ to T11 cord
Metabolic N/A
CSF
Glycine 43.0 μmol/l (1.9–10)
Glutamate 18 μmol/l (0–3.9)
5‐MET 46 nmol/l (72–305)
Lactate 6.69 mmol/l (1.1–2.2)
Plasma
Glycine Normal
Glutamate Normal
Other PAA Normal
Lactate 1.84 mmol/l (0.7–2.1)
Chitotriosidase 500 nmol/hr/ml (0–150)
Palmitoyl thioesterase 12 nmol/hr/mg (17–139)
B‐glucosidase 143 nmol/hr/mg (163–378)
Arylsulfatase A 17 nmol/hr/mg (22–103)
Urine
Glycine 2,393 μmol/l (92–760)
Glutamate 54 μmol/l (0–32)

m, months; y, years; N/A, not applicable; MRS; functional magnetic resonance spectrometry; WM, white matter; SUF, subcortical U fibers; PVWM, periventricular white matter; PLIC, posterior limb of the internal capsule; PB, posterior body; SP, splenium; CC, corpus callosum; CP, cerebral peduncles; DTT, dorsal tegmental tracts; ICP, inferior cerebellar peduncles; CWM, cerebellar white matter; CCJ, craniocervical junction; FP, frontoparietal; OC, occipital; CBH, cerebellar hemispheres; CSF, cerebrospinal fluid; 5‐MET, 5‐methyltetrahydrofolate; PAA, plasma amino acids.