A 16 Years Young Girl with Noonan Syndrome.
Mymensingh Med J
; 29(4): 1004-1009, 2020 Oct.
Article
in En
| MEDLINE
| ID: mdl-33116109
ABSTRACT
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.
Search on Google
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Heart Defects, Congenital
/
Noonan Syndrome
Type of study:
Diagnostic_studies
Limits:
Female
/
Humans
Language:
En
Journal:
Mymensingh Med J
Journal subject:
MEDICINA
Year:
2020
Document type:
Article