Noonan Syndrome with Hepatomegaly and Persistently Elevated Liver Enzymes: A Case Report
نویسندگان
چکیده
Noonan’s syndrome is a polymorphic disorder with some facial features, congenital heart defects, cryptorchidism, etc., and also associated autoimmune diseases, lymphatic dysplasias. Here we are reporting nine years old boy Noonan's who has hepatomegaly persistently raised hepatic enzymes, which remained unexplained.
 TAJ 2022; 35: No-1: 137-140
منابع مشابه
Noonan syndrome: a case report.
Cranio-dento-facial findings in a case of Noonan syndrome in a 13-year, 3-month-old male are reported. Oral examination of the patient revealed a narrow, high arched palate, malocclusion and congenitally missing teeth. Even though cephalometric measurements showed an increased vertical facial pattern (GoGn/SN = 38.46 degrees ), a severe deep bite (9 mm) was evident. Noonan syndrome is character...
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ژورنال
عنوان ژورنال: TAJ
سال: 2022
ISSN: ['1019-8555', '2408-8854']
DOI: https://doi.org/10.3329/taj.v35i1.61168