Abstract
The aim of this study was to assess various aspects of visual function in 6 patients
(age range: 9 months to 7 years and 8 months) with methylmalonic aciduria and homocystinuria.
All patients had an ophthalmological examination and were tested with a battery of
age-appropriate tests assessing various aspects of visual function such as acuity,
visual fields and visual attention. None of the patients had significant retinal abnormalities
but all 6 had nystagmus which was associated with strabismus in 3 of the 6. They all
had some abnormalities on the behavioral tests assessing visual function which appeared
to be related to the age of the patients. Visual impairment was more severe in the
3 patients below 3 years of age and milder in the older patients. The presence and
the severity of abnormalities, in contrast, did not depend on the age at onset or
the age when treatment was started and were only partly related to brain MRI findings.
Severe hydrocephalus and basal ganglia involvement were associated with severe visual
impairment, but abnormal visual findings were also present in the children with normal
MRI and isolated mild periventricular changes. Our results suggest that age, brain
lesions and other factors may be responsible for visual abnormalities in methylmalonic
aciduria and homocystinuria. Further studies using early and sequential assessment
of visual function are needed to establish whether the differences observed between
younger and older children may be related to the duration of therapy.
Key words
Vision - children - homocystinuria - brain - methylmalonic
References
- 1
Atkinson J, Hood B, Wattam-Bell J, Braddick O.
Changes in infants' ability to switch visual attention in the first three months of
life.
Perception.
1992;
21
643-653
- 2 Atkinson J. The Developing Visual Brain. Oxford; Oxford University Press 2000
- 3
Biancheri R, Cerone R, Schiaffino M C, Caruso U, Veneselli E, Perrone M V. et al .
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiological
findings in 14 cases.
Neuropediatrics.
2001;
32
14-22
- 4
Geraghty M T, Perlman E J, Martin L S, Hayflick S J, Casella J F, Rosemblatt D S.
et al .
Cobalamin C defect associated with haemolytic-uremic syndrome.
J Pediatr.
1992;
120
934-937
- 5
Goodman S I, Moe P G, Hammond K B, Mudd S H, Uhlendorf B W.
Homocystinuria with methylmalonic aciduria: two cases in a sibship.
Biochem Med.
1970;
4
500-515
- 6 Griffiths R. The Abilities of Babies. Amersham; Association for Research in Infant
and Child Development 1976
- 7
Mercuri E, Atkinson J, Braddick O, Anker S, Cowan F, Rutherford M. et al .
Basal ganglia damage and impaired visual function in the newborn infant.
Arch Dis Child Fetal Neonatal Ed.
1997;
77
F111-114
- 8
Mercuri E, Atkinson J, Braddick O, Anker S, Cowan F, Rutherford M. et al .
Visual function in full-term infants with hypoxic-ischaemic encephalopathy.
Neuropediatrics.
1997;
28
155-161
- 9
Mercuri E, Anker S, Philpot J, Sewry C, Dubowitz V, Muntoni F.
Visual function in children with merosin-deficient and merosin-positive congenital
muscular dystrophy.
Pediatr Neurol.
1998;
18
399-401
- 10
Mercuri E, Anker S, Guzzetta A, Barnett A L, Haataja L, Rutherford M. et al .
Visual function at school age in children with neonatal encephalopathy and low Apgar
scores.
Arch Dis Child Fetal Neonatal Ed.
2004;
89
F258-262
- 11
Mitchell G A, Watkins D, Melancon S B, Rosenblatt D S, Geoffroy G, Orquin J. et al
.
Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic
aciduria.
J Pediatrics.
1986;
108
410-414
- 12
Mohn G, van Hof-van Duin J.
Development of the binocular and monocular visual field during the first year of life.
Clin Vis Science.
1986;
1
51-64
- 13
Mohn G, van Hof-van Duin J, Fetter W P, de Groot L, Hage M.
Acuity assessment of non-verbal infants and children: clinical experience with the
acuity card procedure.
Dev Med Child Neurol.
1988;
30
232-244
- 14
Robb R M, Bruce Dowton S, Fulton A B, Levy H L.
Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria
and sulfur amino acid abnormalities.
Am J Ophtalmol.
1984;
97
691-696
- 15
Rosenblatt D S, Aspler A L, Shevell M I, Pletcher B A, Fenton W A, Seashore M R.
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria
(cblC).
J Inherit Metab Dis.
1997;
20
528-538
- 16
Rossi A, Cerone R, Biancheri R, Gatti R, Schiaffino M C, Fonda C. et al .
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings.
AJNR Am J Neuroradiol.
2001;
22
554-563
- 17
Shinnar S, Singer H S.
Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence.
N Engl J Med.
1984;
311
451-454
- 18
Suormala T, Baumgartner M R, Coelho D, Zavadakova P, Kozich V, Koch H G. et al .
The cblD defect causes either isolated or combined deficiency of methylcobalamin and
adenosylcobalamin synthesis.
J Biol Chem.
2004;
279
42742-42749
- 19
Teller D Y, McDonald M A, Preston K, Sebris S L, Dobson V.
Assessment of visual acuity in infants and children: the acuity card procedure.
Dev Med Child Neurol.
1986;
26
779-789
- 20
Trabousli E I, Silva J C, Geraghty M T, Maumenee I H, Valle D, Green W R.
Ocular histopathologic characteristics of cobalamin C type vitamin B12 defect with
methylmalonic aciduria and homocystinuria.
Am J Ophthalmol.
1992;
113
269-280
- 21
van Hof-van Duin J, Heersema D J, Groenendaal F, Baerts W, Fetter W PF.
Visual field and grating acuity development in low-risk preterm infants during the
first 2œ years after term.
Behav Brain Res.
1992;
49
115-122
- 22 Wechsler D. Wechsler Preschool and Primary Scale of Intelligence - Revised. Kent;
The Psychological Corporation 1990
Eugenio Mercuri
Istituto di Neuropsichiatria Infantile
Policlinico Gemelli
Largo Gemelli
00168 Roma
Italy
Email: e.mercuri@ic.ac.uk