digeorge syndrome - Axtarish в Google
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13 янв. 2024 г. · DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a condition caused when a small part of chromosome 22 is missing.
DiGeorge syndrome is a condition present from birth that can cause a range of lifelong problems, including heart defects and learning difficulties.
DiGeorge syndrome, also known as 22q11. 2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22.
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, most frequently caused by a deletion at 22q11.2, is a PI caused by abnormal migration and development of certain cells and tissues during ...
14 окт. 2021 г. · Signs and symptoms · Retrognathia or micrognathia · Long face · High and broad nasal bridge · Narrow palpebral fissures · Small teeth.
1 дек. 2019 г. · 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22.
22q11.2 deletion syndrome is a genetic condition that affects many parts of the body. It can cause intellectual disability, learning and social challenges.
Symptoms vary widely and can range from heart defects and developmental delays to seizures. A child's eyes, nose, or ears may look different. Or the child may ...
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