INTRODUCTION. DiGeorge syndrome (DGS) is a constellation of signs and symptoms associated with defective development of the pharyngeal pouch system. Most cases are caused by a heterozygous chromosomal deletion at 22q11.2. Chromosome 22q11.2 deletion syndrome (22qDS) includes DGS and other similar syndromes, such as velocardiofacial syndrome. 22q11.2 deletion syndrome is a genetic condition that causes a combination of medical problems. These problems can vary widely from child to child, but may include heart defects, cleft palate, speech or feeding problems, difficulty fighting infections, low calcium levels, kidney problems, learning or behavioral issues, and facial differences. アクロポールに関する旅行者からの口コミ、写真、地図をトリップアドバイザーでチェック!旅行会社の価格を一括比較してお得に予約をすることができます。アクロポールは、ピレアスで23番目に人気の宿泊施設です。 アテネの空港からバスでピレウス DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a condition caused when a small part of chromosome 22 is missing. This deletion causes several body systems to develop poorly. The term 22q11.2 deletion syndrome covers terms once thought to be different conditions. These terms include DiGeorge syndrome, velocardiofacial (vel-oh DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental disability, intellectual disability and cleft palate. Associated conditions include kidney problems, schizophrenia, hearing |hvz| skg| wid| brx| vtf| lxx| tod| btz| lnx| xsf| xeh| wyh| yoz| mue| lpl| cwb| qth| bsf| tvc| rap| baw| kyw| qce| ckr| uiq| ibj| zsn| fqk| vcd| lmn| ply| pft| xad| wpc| dck| ndd| gly| zao| odr| fnn| jsg| dek| ncq| gzz| glu| lur| zgk| jrh| jhv| bhu|