Literature DB >> 16458828

Expanding the clinical picture of Simpson-Golabi-Behmel syndrome.

Esther L Young1, Robin Wishnow, Michael A Nigro.   

Abstract

This report describes a 14-year-old male with Simpson-Golabi-Behmel overgrowth syndrome. He was born via cesarean section because of macrocephaly and subsequently exhibited significant developmental delay in motor, language, and cognitive skills with mental retardation and epilepsy. He manifests the characteristic dysmorphic ("bulldog") facial features of Simpson-Golabi-Behmel syndrome. His molecular genetic testing has substantiated the clinical diagnosis of Simpson-Golabi-Behmel syndrome; however, he is unique in that he has mental retardation, hydrocephalus, and epilepsy, which have not been previously documented in Simpson-Golabi-Behmel syndrome in the literature.

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Year:  2006        PMID: 16458828     DOI: 10.1016/j.pediatrneurol.2005.07.008

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  5 in total

Review 1.  Beckwith-Wiedemann syndrome and Chiari I malformation--a case-based review of central nervous system involvement in hemihypertrophy syndromes.

Authors:  Suhas Udayakumaran; Chiazor U Onyia
Journal:  Childs Nerv Syst       Date:  2015-02-17       Impact factor: 1.475

2.  Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome.

Authors:  M Bayram; M Yildirim; F Seymen
Journal:  Eur Arch Paediatr Dent       Date:  2014-09-23

Review 3.  Simpson-Golabi-Behmel syndrome types I and II.

Authors:  Jair Tenorio; Pedro Arias; Víctor Martínez-Glez; Fernando Santos; Sixto García-Miñaur; Julián Nevado; Pablo Lapunzina
Journal:  Orphanet J Rare Dis       Date:  2014-09-20       Impact factor: 4.123

4.  SGBS cells as a model of human adipocyte browning: A comprehensive comparative study with primary human white subcutaneous adipocytes.

Authors:  Chia Rou Yeo; Madhur Agrawal; Shawn Hoon; Asim Shabbir; Manu Kunaal Shrivastava; Shiqi Huang; Chin Meng Khoo; Vanna Chhay; M Shabeer Yassin; E Shyong Tai; Antonio Vidal-Puig; Sue-Anne Toh
Journal:  Sci Rep       Date:  2017-06-22       Impact factor: 4.379

Review 5.  Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Authors:  Jing Liu; Qin Liu; Shuting Yang; Na Ma; Jialun Pang; Ying Peng; Hui Xi; Zhengjun Jia; Yingchun Luo; Meiping Jiang; Yanling Teng; Wenxian Yu; Zhuo Li; Hua Wang
Journal:  Mol Genet Genomic Med       Date:  2021-07-22       Impact factor: 2.183

  5 in total

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