Mutation analysis of a family with 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 783-786, 2013.
Article
in Zh
| WPRIM
| ID: wpr-275622
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>The aim of this study was to explore the genetic features of a family with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBDD) which may provide the basis for the diagnosis and genetic counseling.</p><p><b>METHOD</b>Clinical data of the proband was collected, total RNA and genomic DNA were extracted from the peripheral blood. The whole coding region of the ACAT1 gene was amplified by RT-PCR. 5' noncoding region of the ACAT1 gene and all 6 exons and flanking intron regions of the HADH2 gene were amplified by PCR. All amplification products were directly sequenced and compared with the reference sequence.</p><p><b>RESULT</b>(1) The patient was a one-year-old boy who presented with psychomotor retardation and astasia when he was admitted to the hospital. Biochemical test revealed slight hyperlactatemia (3.19 mmol/L) and magnetic resonance imaging showed delayed myelination. 2-Methylacetoacetyl-CoA thiolase deficiency was suggested by gas chromatography-mass spectrometry. (2) There was no mutation in the ACAT1 gene and a hemizygous missense mutation c.388C > T was found in the 4 exon of the HADH2 gene which resulted in p. R130C. Proband's mother was the heterozygote and the father was normal.</p><p><b>CONCLUSION</b>This is the first report on MHBDD patient and HADH2 mutation in China. p.R130C is responsible for the pathogenesis of the disease in the infant.</p>
Full text:
1
Database:
WPRIM
Main subject:
Pathology
/
Pedigree
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Acetyl-CoA C-Acetyltransferase
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Acyl Coenzyme A
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DNA Mutational Analysis
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Base Sequence
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Reverse Transcriptase Polymerase Chain Reaction
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Mutation, Missense
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Dyskinesias
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Mental Retardation, X-Linked
Limits:
Humans
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Infant
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Male
Language:
Zh
Journal:
Chinese Journal of Pediatrics
Year:
2013
Document type:
Article