beckwith-wiedemann syndrome - Axtarish в Google
3 дек. 2021 г. · Beckwith-Wiedemann syndrome is a condition that affects many parts of the body. Explore symptoms, inheritance, genetics of this condition.
BWS is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features.
Синдром Беквита — Видемана
Синдром Беквита — Видемана — одна из редких генетических аномалий, связана с превышением норм роста плода при беременности и с несогласованным развитием различных отделов организма. Википедия
МКБ-10-КМ : Q87.3
OMIM : 130650
Beckwith-Wiedemann syndrome is a genetic disorder that can cause an overgrowth of particular body parts. Learn more from Boston Children's Hospital.
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder characterized by overgrowth. The syndrome occurs in 1 in 11000 births. What is Beckwith-Wiedemann... · Causes · Treatment
Beckwith-Wiedemann Syndrome (BWS) is a genetic disorder that affects your child's growth and increases their risk of developing certain childhood cancers.
Beckwith-Wiedemann syndrome (BWS) is a congenital (present at birth) overgrowth syndrome that occurs in approximately one in 15,000 births.
Beckwith-Wiedemann syndrome (BWS) is the most common overgrowth and cancer predisposition disorder. BWS is caused by changes on chromosome 11p15.5 and is ...
1 мая 2024 г. · BWS is a pediatric cancer predisposition disorder caused by changes in the imprinted gene loci on chromosome 11p15. Patients develop BWS as a ...
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