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“Supravalvular Aortic Stenosis”, Victor McKusick, Mendelian Inheritance in Man, 1966. (SVAS) 瓣膜上主動脈狹窄。icd10=Q25.3

Genomic coordinate 7:74,028,173


Here I present: Supravalvular Aortic Stenosis”, Victor McKusick, Mendelian Inheritance in Man’, 1966. (SVAS瓣膜上主動脈狹窄icd10=Q25.3

INTRODUCTION.

Supravalvular aortic stenosis (SVAS) is a congenital obstructive narrowing of the aorta just above the aortic valve and is the least common type of aortic stenosis. It is often associated with other cardiovascular anomalies and is one of the characteristic findings of Williams syndrome. The diagnosis can be made by echocardiography or MRI.

There is evidence supravalvular aortic stenosis (SVAS) is caused by heterozygous mutation in the gene encoding elastin (ELN) on cytogenetic location  7q11.23 and genomic coordinates 7:74,028,173-74,069,907.  The screenshot of the ELN gene 41,735 bp (base pairs) of DNA sequence length is shown BELOW.  Nine (9) other genes besides ELN in the 7q11.23 cytogenetic location are listed BENEATH. 

 



 

Coordinate  Symbol  Genomic Name
7:73,768,997  CLDN3 Claudin-3 
7:73,830,996  CLDN4 Claudin 4
7:73,834,590  WBSCR27 Williams-Beuren syndrome chromosome region 27
7:73,860,848  WBSCR28 Williams-Beuren syndrome chromosome region 28
7:74,028,173  ELN Elastin
7:74,083,804  LIMK1 LIM domain kinase 1
7:74,174,356  EIF4H Eukaryotic translation initiation factor 4H
7:74,191,198  MIR590 Micro RNA 590
7:74,210,006  LAT2 Linker for activation of T cells family, member 2
7:74,231,502  RFC2 Replication factor C2

 

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