Author:
Liu Yu,Yang Ying,Chu Liming,Ren Shuai,Li Ying,Gao Aimin,Wen Jing,Deng Wanling,Lu Yan,Kong Lingyin,Liang Bo,Shao Xiaoshan
Abstract
Interstitial chromosome 20q deletions, containing GNAS imprinted locus, are rarely reported in the past. Hereby, we presented a Chinese boy with a novel 4.36 Mb deletion at paternal 20q13.2-13.32, showing feeding difficulty, malnutrition, short stature, lower limb asymmetry, sightly abnormal facial appearance and mild intellectual abnormality. With 3 years’ growth hormone treatment, his height was increased from 90 to 113.5 cm. This report is the first time to describe the outcome of clinical treatment on a patient with this rare chromosomal 20 long arm interstitial deletion, containing GNAS locus, which may facilitate the diagnosis and treatment of this type of patient in the future.
Subject
Genetics (clinical),Genetics,Molecular Medicine
Cited by
1 articles.
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