Your browser doesn't support javascript.
loading
A 16 Years Young Girl with Noonan Syndrome.
Chowdhury, M T; Sheikh, N; Haque, M; Shakil, S S; Tanni, A Z.
Affiliation
  • 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.
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.
Subject(s)
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
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