Beckwith-Wiedemann syndrome - Genetics - MedlinePlus medlineplus.gov › Genetics › Genetic Conditions
3 дек. 2021 г. · Beckwith-Wiedemann syndrome is a condition that affects many parts of the body. Explore symptoms, inheritance, genetics of this condition. |
21 сент. 2023 г. · Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia, macrosomia, ... Figure 2. [Causes of Beckwith... · GeneReviews · Treatment of Manifestations]. |
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 genetic disorder that affects your child's growth and increases their risk of developing certain childhood cancers. BWS, ... |
Beckwith-Wiedemann syndrome (BWS) is the most common overgrowth and cancer predisposition disorder. BWS is caused by changes on chromosome 11p15.5 and is ... |
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder characterized by overgrowth. The syndrome occurs in 1 in 11000 births. |
BWS is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features. Presentation · Genetics · Management · Epidemiology |
| 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 (BWS) is a congenital (present at birth) overgrowth syndrome that occurs in approximately one in 15,000 births. |
Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations. ORPHA:116. |
| Novbeti > |
| Axtarisha Qayit Anarim.Az Anarim.Az Sayt Rehberliyi ile Elaqe Saytdan Istifade Qaydalari Anarim.Az 2004-2023 |