Literature DB >> 1728538

Metabolic pigmentary retinopathies: diagnosis and therapeutic attempts.

B T Poll-The1, T Billette de Villemeur, M Abitbol, J L Dufier, J M Saudubray.   

Abstract

Retinal degeneration in children occurs in errors of lipid, peroxisomal and mitochondrial (including respiratory chain) metabolism. In this review the most frequent inborn errors of metabolism with retinal degeneration are discussed including abetalipoproteinaemia, classical Refsum disease, neuronal ceroid lipofuscinosis, hydroxydicarboxylic aciduria, Sjögren-Larsson syndrome, infantile Refsum disease, Kearns-Sayre syndrome and gyrate atrophy. These metabolic disorders must be differentiated from those with retinal degeneration but without known metabolic basis. In patients with such a disorder metabolic investigations should be considered whenever atypical manifestations are encountered.

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Year:  1992        PMID: 1728538     DOI: 10.1007/bf02073880

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


  23 in total

1.  Oligophrenia in combination with congenital ichthyosis and spastic disorders; a clinical and genetic study.

Authors:  T SJOGREN; T LARSSON
Journal:  Acta Psychiatr Neurol Scand Suppl       Date:  1957

2.  Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

Authors:  B T Poll-The; J P Bonnefont; H Ogier; C Charpentier; A Pelet; J M Le Fur; C Jakobs; R M Kok; M Duran; P Divry
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

4.  Raised plasma-ornithine and gyrate atrophy of the choroid and retina.

Authors:  O Simell; K Takki
Journal:  Lancet       Date:  1973-05-12       Impact factor: 79.321

5.  Vitamin A and vitamin E replacement in abetalipoproteinemia.

Authors:  J G Bieri; J M Hoeg; E J Schaefer; L A Zech; H B Brewer
Journal:  Ann Intern Med       Date:  1984-02       Impact factor: 25.391

6.  Mitochondrial oxidation of phytanic acid in human and monkey liver: implication that Refsum's disease is not a peroxisomal disorder.

Authors:  P A Watkins; S J Mihalik
Journal:  Biochem Biophys Res Commun       Date:  1990-03-16       Impact factor: 3.575

7.  A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Authors:  T P Dryja; T L McGee; E Reichel; L B Hahn; G S Cowley; D W Yandell; M A Sandberg; E L Berson
Journal:  Nature       Date:  1990-01-25       Impact factor: 49.962

8.  A progressive neurologic syndrome in children with chronic liver disease.

Authors:  J L Rosenblum; J P Keating; A L Prensky; J S Nelson
Journal:  N Engl J Med       Date:  1981-02-26       Impact factor: 91.245

9.  Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence.

Authors:  D N Palmer; R D Martinus; S M Cooper; G G Midwinter; J C Reid; R D Jolly
Journal:  J Biol Chem       Date:  1989-04-05       Impact factor: 5.157

10.  Patterns of Refsum's disease. Phytanic acid oxidase deficiency.

Authors:  A Poulos; A C Pollard; J D Mitchell; G Wise; G Mortimer
Journal:  Arch Dis Child       Date:  1984-03       Impact factor: 3.791

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  5 in total

1.  Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency.

Authors:  I Schrijver-Wieling; G H van Rens; D Wittebol-Post; J A Smeitink; J P de Jager; H B de Klerk; G H van Lith
Journal:  Br J Ophthalmol       Date:  1997-04       Impact factor: 4.638

2.  Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patients.

Authors:  A Fiumara; R Barone; P Buttitta; M Di Pietro; A Scuderi; F Nigro; J Jaeken
Journal:  Br J Ophthalmol       Date:  1994-11       Impact factor: 4.638

3.  Neuronal ceroid lipofuscinosis in the Polish Owczarek Nizinny (PON) dog. A retinal study.

Authors:  A Wrigstad; S E Nilsson; R Dubielzig; K Narfström
Journal:  Doc Ophthalmol       Date:  1995       Impact factor: 2.379

Review 4.  The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overview.

Authors:  Àngels Garcia-Cazorla; Fanny Mochel; Foudil Lamari; Jean-Marie Saudubray
Journal:  J Inherit Metab Dis       Date:  2014-11-21       Impact factor: 4.982

Review 5.  Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Authors:  Aymane Bouzidi; Hicham Charoute; Majida Charif; Ghita Amalou; Mostafa Kandil; Abdelhamid Barakat; Guy Lenaers
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

  5 in total

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