Literature DB >> 2606126

Hyperprolinaemia type I and white matter disease: coincidence or causal relationship?

M Steinlin1, E Boltshauser, B Steinmann, W Wichmann, G Niemeyer.   

Abstract

We describe a 10-year-old boy with hyperprolinaemia type I and severe neurological abnormalities (mental retardation, cerebral palsy, epilepsy, nystagmus). Magnetic resonance imaging showed diffuse white matter involvement and electroretinography confirmed tapetoretinal degeneration. In view of reports in the literature, hyperprolinaemia type I may not be a benign condition, as usually assumed, but may lead to marked neurological abnormalities, particularly in affected males.

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Year:  1989        PMID: 2606126     DOI: 10.1007/bf02024332

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  16 in total

1.  HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.

Authors:  H KOPELMAN; A M ASATOOR; M D MILNE
Journal:  Lancet       Date:  1964-11-21       Impact factor: 79.321

2.  FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.

Authors:  M L EFRON
Journal:  N Engl J Med       Date:  1965-06-17       Impact factor: 91.245

3.  Type I hyperprolinemia in a family suffering from aniridia and severe dystrophia of ocular tissues.

Authors:  G Fusco; S Carlomagno; A Romano; E Rinaldi; G Cedrola; L Cianciaruso; A Curto; S Rosolia; G Auricchio
Journal:  Ophthalmologica       Date:  1976       Impact factor: 3.250

4.  Hyperprolinemia: clinical and biochemical family study.

Authors:  N C Woody; C H Snyder; J A Harris
Journal:  Pediatrics       Date:  1969-10       Impact factor: 7.124

5.  Hereditary renal disease with neurosensory hearing loss, prolinuria and ichthyosis.

Authors:  R A Goyer; J Reynolds; J Burke; P Burkholder
Journal:  Am J Med Sci       Date:  1968-09       Impact factor: 2.378

6.  [Type I hyperprolinemia. Study of a familial case].

Authors:  G Fontaine; J P Farriaux; M Dautrevaux
Journal:  Helv Paediatr Acta       Date:  1970-04

7.  [Familial essential hyperprolinemia].

Authors:  H Hainaut; J Hariga; C Willems; A Heusden; P Chapelle
Journal:  Presse Med       Date:  1971-04-24       Impact factor: 1.228

8.  Hyperprolinaemia and gyrate atrophy of the choroid and retina in members of the same family.

Authors:  E P Douglas
Journal:  Br J Ophthalmol       Date:  1985-08       Impact factor: 4.638

9.  Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.

Authors:  I A Schafer; C R Scriver; M L Efron
Journal:  N Engl J Med       Date:  1962-07-12       Impact factor: 91.245

10.  [Information conveyed by electroretinography (author's transl)].

Authors:  G Niemeyer
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1979-08
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  3 in total

Review 1.  Behavioral and neurochemical effects of proline.

Authors:  Angela T S Wyse; Carlos Alexandre Netto
Journal:  Metab Brain Dis       Date:  2011-06-04       Impact factor: 3.584

Review 2.  Neuroradiological and neurophysiological indices for neurometabolic disorders.

Authors:  A Kohlschütter
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

3.  Biochemical and clinical features of hereditary hyperprolinemia.

Authors:  Hiroshi Mitsubuchi; Kimitoshi Nakamura; Shirou Matsumoto; Fumio Endo
Journal:  Pediatr Int       Date:  2014-08       Impact factor: 1.524

  3 in total

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