DiGeorge syndrome is a condition present from birth that can cause a range of lifelong problems, including heart defects and learning difficulties. |
| Синдром Ди Георга Заболевание |
Синдром Ди Георга — разновидность идиопатического изолированного гипопаратиреоза; редкое врождённое заболевание. Генетической причиной синдрома Ди Георга является делеция центрального участка длинного плеча хромосомы 22 размером 1.5-3 млн.п.н. Википедия
МКБ-10 : D82.1
МКБ-11 : LD44.N0
МКБ-9 : 279.11, 758.32
OMIM : 188400
DiGeorge syndrome is a genetic condition caused by a missing piece of chromosome 22. Another name for DiGeorge syndrome is 22q11.2 deletion syndrome. |
DiGeorge Syndrome (DGS) is a combination of signs and symptoms caused by defects in the development of structures derived from the pharyngeal arches during ... |
14 окт. 2021 г. · Signs and symptoms · Retrognathia or micrognathia · Long face · High and broad nasal bridge · Narrow palpebral fissures · Small teeth. |
DiGeorge syndrome is a primary immunodeficiency disorder that involves T cell defects. It results from gene deletions in the DiGeorge chromosomal region at 22q ... |
What are the symptoms of 22q11.2 deletion? · heart problems · low muscular tone · speech difficulties · middle ear infections or hearing loss · vision problems ... |
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