| Autor: |
Chowdhury MT; Dr MSI Tipu Chowdhury, Junior Consultant, Department of Cardiology, Cox's Bazar Medical College Hospital, Cox's Bazar, Bangladesh; E-mail: dr.tipuchowdhury@gmail.com., Sheikh N, Haque M, Shakil SS, Tanni AZ |
| Jazyk: |
angličtina |
| Zdroj: |
Mymensingh medical journal : MMJ [Mymensingh Med J] 2020 Oct; Vol. 29 (4), pp. 1004-1009. |
| Abstrakt: |
Noonan's syndrome is a developmental disorder characterized by short stature, typical facial dysmorphia, congenital heart defects and skeletal deformity. It may be sporadic or inherited as an autosomal dominant or recessive trait which occurs, one in 1000-2500 live births. We report a case of 16 years young girl presented to the hospital with short stature, Shortness of breath, morphologic features and congenital heart defect of Noonan Syndrome who has no similar history in the family and admitted in Bangabandhu Sheikh Mujib Medical University on 12th August 2018. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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