Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA
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- 作者：Namik Kaya ; Mohammad Al-Owain ; AlB ; ary AlBakheet ; Dilek Colak ; Ali Al-Odaib ; Faiqa Imtiaz ; Serdar Coskun ; Moeenaldeen Al-Sayed ; Zuhair Al-Hassnan ; Hamad Al-Zaidan ; Brian Meyer ; Pinar Oz
- 关键词：Propionic acidemia ; PCCA ;
; //www.sciencedirect.com/scidirimg/entities/223c.gif"" alt=""not ; vert ; similar"" title=""not ; vert ; similar"" border=""0"">73 kb Deletion ; 18 bp Intronic insertion ; aCGH
- 刊名：European Journal of Medical Genetics
- 出版年：2008
- 出版时间：November-December 2008
- 年：2008
- 卷：51
- 期：6
- 页码：558-565
- 全文大小：336 K
文摘
Propionic acidemia is a metabolic disorder (OMIM 606054) caused by deficiency of the propionyl-coenzyme A (CoA) carboxylase, which subsequently results in accumulation of propionic acid. Patients may initially present with poor feeding, vomiting, loss of appetite, hypotonia, and lethargy. Later, most children will show different degrees of motor, social and language delay even more serious medical problems, including heart abnormalities, seizures, coma, and possibly death. Two siblings affected with propionic acidemia were screened for putative mutations in PCCA and PCCB genes coding α and β subunits of propionyl-coenzyme A (CoA) carboxylase, respectively. Both patients had a mild–severe form of propionic acidemia. The investigations using PCR, long-PCR, array comparative genomic hybridization (aCGH), and sequencing techniques showed a 73 kb deletion extending from intron 16 to intron 19 and an 18 bp insertion at the distal end of the deletion in PCCA gene. The deletion so far is the largest gross change reported in the literature for the PCCA gene.