Asthma Allergy Immunology

Asthma Allergy Immunology

2016, Vol 14, Num, 3     (Pages: 129-142)

DiGeorge Syndrome

Bahar Göktürk 1, İsmail Reisli 2,

1 Başkent Üniversitesi Konya Uygulama ve Araştırma Merkezi, Çocuk Allerji ve İmmünoloji Bölümü, Konya, Türkiye
2 Necmettin Erbakan Üniversitesi Meram Tıp Fakültesi, Çocuk Allerji ve İmmünoloji Bilim Dalı, Konya, Türkiye

DOI: 10.21911/aai.5013
Viewed: 643
Downloaded : 441

DiGeorge syndrome, which is caused by abnormal development and migration of neural crest cells, is the most common microdeletion syndrome. The phenotype is variable due to the existence of more than 35 genes in the typical deletion region. However, the genotypephenotype correlation is very weak in this patient group. Every patient with facial dysmorphism, delay in developmental milestones and macrothrombocytopenia should be questioned for the other specific findings of DGS, and tested if needed. All findings do not have to be together to make the diagnosis. It should be known that patients experience different problems at different stages of their lives, and genetic counseling should be provided to the patients and their families. Our aim in this review was to provide detailed information and raise awareness about DGS as it is common but rarely diagnosed, and presents many difficulties during follow-up.

Keywords : DiGeorge syndrome, Hypoparathyroidism, Conotruncal- cardiac defect, Macrothrombocytopenia