Literature DB >> 9143889

Ascorbic acid and amino acid values in the aqueous humor of a patient with Lowe's syndrome.

S Hayasaka1, T Yamada, K Nitta, Y Kaji, S Hiraki, K Tachinami, M Matsumoto, S Yamamoto, S Yamamoto.   

Abstract

BACKGROUND: Aminoaciduria is found in Lowe's syndrome. No studies of concentrations of ascorbic acid and amino acids in the aqueous humor of the syndrome have been performed. We examined these concentrations in a patient with Lowe's syndrome.
METHODS: Ascorbic acid and amino acid levels in the aqueous humor and plasma of a male infant were measured by means of high-performance liquid chromatography. The patient, who had congenital cataract, miotic pupils, opaque corneas, glaucoma, aminoaciduria, normal levels of ascorbic acid and amino acid in the plasma, and renal tubular acidosis, underwent trabeculotomy, lensectomy, and anterior vitrectomy in both eyes.
RESULTS: Intraocular pressure in both eyes decreased to within the normal range, but both corneas remained opaque. The amino acid levels in the aqueous humor were similar to those in the plasma, but intracameral ascorbic acid levels were decreased. After topical instillation of ascorbic acid, the corneas became transparent. The proband's mother had good visual acuity but paracentral lens opacities in both eyes. His maternal grandmother had scattered cortical opacities in both lenses.
CONCLUSION: In this infant with Lowe's syndrome, we found intracameral levels of amino acids similar to those in the plasma. Levels of ascorbic acid in the aqueous humor were decreased.

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Year:  1997        PMID: 9143889     DOI: 10.1007/bf00941762

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  19 in total

1.  Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity.

Authors:  C U LOWE; M TERREY; E A MacLACHLAN
Journal:  AMA Am J Dis Child       Date:  1952-02

2.  Ocular manifestations in patients and female relatives of families with the oculocerebrorenal syndrome of Lowe.

Authors:  S S Johnston; N C Nevin
Journal:  Birth Defects Orig Artic Ser       Date:  1976

3.  Lowe syndrome: identification of the carrier state.

Authors:  N Brown; R J Gardner
Journal:  Birth Defects Orig Artic Ser       Date:  1976

4.  Ion-exchange chromatography of free amino acids in human intraocular fluids.

Authors:  D G Durham; J C Dickinson; P B Hamilton
Journal:  Clin Chem       Date:  1971-04       Impact factor: 8.327

5.  Endogenous renal transport of free amino acids in infancy and childhood.

Authors:  J Brodehl; K Gellissen
Journal:  Pediatrics       Date:  1968-09       Impact factor: 7.124

6.  Ion exchange chromatography of free amino acids in aqueous fluid and lens of the human eye.

Authors:  J C Dickinson; D G Durham; P B Hamilton
Journal:  Invest Ophthalmol       Date:  1968-10

7.  Uptake of proline in cultured cells from patients with Lowe's syndrome.

Authors:  B States; M J Palmieri; S Segal
Journal:  Biochem Biophys Res Commun       Date:  1982-11-30       Impact factor: 3.575

8.  Mitochondrial defects in Lowe's oculocerebrorenal syndrome.

Authors:  J M Gobernado; M Lousa; A Gimeno; M Gonsalvez
Journal:  Arch Neurol       Date:  1984-02

Review 9.  Biochemical studies on Lowe's syndrome.

Authors:  I Yamashina; H Yoshida; S Fukui; I Funakoshi
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

Review 10.  Ascorbic acid and the eye.

Authors:  D L Garland
Journal:  Am J Clin Nutr       Date:  1991-12       Impact factor: 7.045

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  1 in total

1.  Ascorbic acid concentrations in aqueous humor after systemic vitamin C supplementation in patients with cataract: pilot study.

Authors:  Young-Sool Hah; Hye Jin Chung; Sneha B Sontakke; In-Young Chung; Sunmi Ju; Seong-Wook Seo; Ji-Myong Yoo; Seong-Jae Kim
Journal:  BMC Ophthalmol       Date:  2017-07-11       Impact factor: 2.209

  1 in total

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