The clinical and molecular spectrum of galactosemia in patients from the Cape Town region of South AfricaReport as inadecuate




The clinical and molecular spectrum of galactosemia in patients from the Cape Town region of South Africa - Download this document for free, or read online. Document in PDF available to download.

BMC Pediatrics

, 2:7

First Online: 02 September 2002Received: 19 July 2002Accepted: 02 September 2002

Abstract

BackgroundThe objective of this study was to document the clinical, laboratory and genetic features of galactosemia in patients from the Cape Town metropolitan region.

MethodsDiagnoses were based on thin layer chromatography for galactosuria-galactosemia and assays of erythrocyte galactose-1-phosphate uridyltransferase GALT and galactokinase activities. Patients were screened for the common S135L and Q188R transferase gene mutations, using PCR-based assays. Screening for the S135L mutation in black newborns was used to estimate the carrier rate for galactosemia in black South Africans.

ResultsA positive diagnosis of galactosemia was made in 17 patients between the years 1980 to 2001. All had very low or absent galactose-1-phosphate uridyltransferase GALT activity, and normal galactokinase levels. The mean age at diagnosis was 5.1 months range 4 days to 6.5 months. A review of 9 patients showed that hepatomegaly 9-9, and splenomegaly, failure to thrive, developmental delay, bilateral cataracts 6-9 were the most frequent features at diagnosis. Six had conjugated hyperbilirubinemia. Four experienced invasive E. coli infection before diagnosis. Ten patients were submitted to DNA analysis. All 4 black patients and 2 of mixed extraction were homozygous for the S135L allele, while all 3 white patients were homozygous for the Q188R allele. The remaining patient of mixed extraction was heterozygous for the Q188R allele. The estimated carrier frequency of the S135L mutation in 725 healthy black newborns was 1-60.

ConclusionsIn the absence of newborn screening the delay in diagnosis is most often unacceptably long. Also, carrier frequency data predict a galactosemia incidence of approximately 1-14 400 for black newborns in the Cape Metropole, which is much higher than the current detection rate. It is thus likely that many patients go undetected.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2431-2-7 contains supplementary material, which is available to authorized users.

Download fulltext PDF



Author: Howard Henderson - Felicity Leisegang - Ruth Brown - Brian Eley

Source: https://link.springer.com/



DOWNLOAD PDF




Related documents