Literature DB >> 6864396

Identification of female carriers of adrenoleukodystrophy.

H W Moser, A E Moser, J E Trojak, S W Supplee.   

Abstract

The concentrations of very long chain fatty acids in plasma and cultured skin fibroblasts were studied in 96 women who were obligate heterozygotes for X-linked adrenoleukodystrophy, in 34 women who were mothers of single probands with ALD, and in 32 normal women of comparable age. Discriminant analysis was used to develop a classification function for the plasma values. With this function, plasma values in 88% of the women who were obligate heterozygotes for ALD and 77% of the mothers of single probands were identified as abnormal. With subsequent inclusion of the fibroblast assay data, abnormal plasma values were found in 93% of the obligate heterozygotes.

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Year:  1983        PMID: 6864396     DOI: 10.1016/s0022-3476(83)80775-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  22 in total

Review 1.  X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy.

Authors:  B M van Geel; J Assies; R J Wanders; P G Barth
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-07       Impact factor: 10.154

2.  Adrenoleucodystrophy: a molecular genetic study in five families.

Authors:  R G Del Mastro; S Bundey; M W Kilpatrick
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

3.  A family with adrenoleucodystrophy.

Authors:  R P Singh; S Deshpande; R K Marwaha; K Garg
Journal:  Indian J Pediatr       Date:  1989 Sep-Oct       Impact factor: 1.967

4.  Adrenoleukodystrophy in a mother and son.

Authors:  R H Simpson; J Rodda; C J Reinecke
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-09       Impact factor: 10.154

5.  Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

Authors:  B A van Oost; P M van Zandvoort; W Tünte; H G Brunner; A J Hoogeboom; P D Maaswinkel-Mooy; J Bakkeren; B Hamel; H H Ropers
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

6.  Decreasing serum VLCFA levels in ageing X-ALD female carriers.

Authors:  T J Stradomska; A Tylki-Szymańska
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

7.  First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe.

Authors:  J Boué; I Oberle; R Heilig; J L Mandel; A Moser; H Moser; J W Larsen; Y Dumez; A Boué
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 8.  Peroxisomal disorders: a newly recognised group of genetic diseases.

Authors:  R B Schutgens; H S Heymans; R J Wanders; H van den Bosch; J M Tager
Journal:  Eur J Pediatr       Date:  1986-02       Impact factor: 3.183

9.  Pharmacological Complementation Remedies an Inborn Error of Lipid Metabolism.

Authors:  Meredith D Hartley; Mitra D Shokat; Margaret J DeBell; Tania Banerji; Lisa L Kirkemo; Thomas S Scanlan
Journal:  Cell Chem Biol       Date:  2020-03-12       Impact factor: 8.116

10.  Color vision defects in adrenomyeloneuropathy.

Authors:  G H Sack; M B Raven; H W Moser
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025

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