Literature DB >> 3561956

Ophthalmologic manifestations of X-linked childhood adrenoleukodystrophy.

E I Traboulsi, I H Maumenee.   

Abstract

The ophthalmologic findings in 15 patients with childhood adrenoleukodystrophy (ALD) are reviewed. In this X-linked demyelinating disease with adrenal dysfunction, relentlessly progressive visual loss followed by optic atrophy occurs months to years after the diagnosis is established based on neurologic symptoms and biochemical abnormalities. Visual loss is mainly due to central nervous system (CNS) demyelination involving the visual tracts, but primary retinal ganglion cell degeneration may also be operative. All patients in this study were male. Vision ranged from 20/20 to no light perception (NLP). All but one patient with bilateral cataracts had normal anterior segment examinations. Seven patients had exotropia, and esotropia developed in one patient. Electroretinography (ERG) and electrooculography (EOG) findings were normal in two patients with severe visual loss. Macular pigmentary changes were observed in three patients. Optic pallor was noticed in seven patients. Optic nerve hypoplasia was seen in one patient. Visual-evoked responses were abnormal in two patients and borderline in one. Progressive visual field abnormalities were noticed in three patients, large field cuts in two patients, and normal fields in another two patients. The diagnosis of ALD should be considered in all boys presenting with unexplained visual loss, dementia, and adrenal dysfunction.

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Year:  1987        PMID: 3561956     DOI: 10.1016/s0161-6420(87)33504-3

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  5 in total

1.  The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?

Authors:  R G Gray; S H Green; P Davies; S Alger; A Green
Journal:  J Inherit Metab Dis       Date:  1999-08       Impact factor: 4.982

2.  Pigmentary retinopathy, macular oedema, and abnormal ERG with mitotane treatment.

Authors:  W T Ng; M G Toohey; L Mulhall; D A Mackey
Journal:  Br J Ophthalmol       Date:  2003-04       Impact factor: 4.638

3.  Retinal Ganglion Cell Loss in X-linked Adrenoleukodystrophy with an ABCD1 Mutation (Gly266Arg).

Authors:  Yasuhiro Ohkuma; Takaaki Hayashi; Syouyou Yoshimine; Hiroshi Tsuneoka; Yoko Terao; Masaharu Akiyama; Hiroyuki Ida; Toya Ohashi; Akihisa Okumura; Nobuyuki Ebihara; Akira Murakami; Nobuyuki Shimozawa
Journal:  Neuroophthalmology       Date:  2014-10-09

Review 4.  Ophthalmic manifestations of inherited neurodegenerative disorders.

Authors:  Hannah M Kersten; Richard H Roxburgh; Helen V Danesh-Meyer
Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

5.  Optic nerve demyelination as the presenting feature of adrenoleukodystrophy in a child.

Authors:  Nirupama Kasturi; Sandip Sarkar; Tanmay Gokhale; Chinnaiah G Delhikumar; Midhusha R Vendoti
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

  5 in total

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