Literature DB >> 25642806

Bilateral frontoparietal polymicrogyria: a novel GPR56 mutation and an unusual phenotype.

Rita Santos-Silva1, Armanda Passas1, Carla Rocha1, Rita Figueiredo2, Jose Mendes-Ribeiro3, Susana Fernandes4, Saskia Biskup5, Miguel Leão6.   

Abstract

Loss of function of GPR56 causes a specific brain malformation called the bilateral frontoparietal polymicrogyria (BFPP), which has typical clinical and neuroradiological findings. So far, 35 families and 26 independent mutations have been described.We present a Portuguese 5-year-old boy, born from nonconsanguineous parents, with BFPP. This patient has a novel GPR56 mutation (R271X) and an unusual phenotype, because he presents hot water epilepsy.To the best of our knowledge, this is the first reported case of BFPP evolving hot water epilepsy. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2015        PMID: 25642806     DOI: 10.1055/s-0034-1399754

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  8 in total

1.  Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families.

Authors:  Humaira Aziz Sawal; Ricardo Harripaul; Anna Mikhailov; Kayla Vleuten; Farooq Naeem; Tanveer Nasr; Muhammad Jawad Hassan; John B Vincent; Muhammad Ayub; Muhammad Arshad Rafiq
Journal:  J Pediatr Genet       Date:  2017-12-21

2.  Rare SLC1A1 variants in hot water epilepsy.

Authors:  Kalpita Rashimi Karan; P Satishchandra; Sanjib Sinha; Anuranjan Anand
Journal:  Hum Genet       Date:  2017-03-21       Impact factor: 4.132

3.  Disease-associated extracellular loop mutations in the adhesion G protein-coupled receptor G1 (ADGRG1; GPR56) differentially regulate downstream signaling.

Authors:  Ayush Kishore; Randy A Hall
Journal:  J Biol Chem       Date:  2017-04-19       Impact factor: 5.157

4.  Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556.

Authors:  Edmund S Cauley; Ahlam Hamed; Inaam N Mohamed; Maha Elseed; Samantha Martinez; Ashraf Yahia; Fatima Abozar; Rayan Abubakr; Mahmoud Koko; Liena Elsayed; Xianhua Piao; Mustafa A Salih; M Chiara Manzini
Journal:  Neurogenetics       Date:  2019-04-13       Impact factor: 2.660

5.  Two Novel Compound Heterozygous ADGRG1/GPR56 Mutations Associated with Diffuse Cerebral Polymicrogyria.

Authors:  Ruchika Jha; Uday B Kovilapu; Amit Devgan; Vishal Sondhi
Journal:  J Pediatr Genet       Date:  2020-07-29

6.  White-Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations.

Authors:  Sevim Türay; Recep Eröz
Journal:  Acta Neurol Belg       Date:  2021-04-10       Impact factor: 2.471

7.  Novel compound heterozygous GPR56 gene mutation in a twin with lissencephaly: A case report.

Authors:  Wen-Xin Lin; Ying-Ying Chai; Ting-Ting Huang; Xia Zhang; Guo Zheng; Gang Zhang; Fang Peng; Yan-Jun Huang
Journal:  World J Clin Cases       Date:  2022-01-14       Impact factor: 1.337

8.  Personality Changes in Bilateral Superior Frontal and Parafalcine Frontoparietal Polymicrogyria: A Rare Case Report.

Authors:  Astha Singh; Hardeep Singh Malhotra; Adarsh Tripathi; Sujita Kumar Kar
Journal:  Indian J Psychol Med       Date:  2018 Mar-Apr
  8 in total

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