Literature DB >> 30497210

A familial syndrome of hypothalamic hamartomas, polydactyly, and SMO mutations: a clinical report of 2 cases.

Sebastian Rubino1, Jiang Qian2, Carlos D Pinheiro-Neto3, Tyler J Kenning1, Matthew A Adamo1.   

Abstract

Hypothalamic hamartomas are benign tumors known to cause gelastic or dacrystic seizures, precocious puberty, developmental delay, and medically refractory epilepsy. These tumors are most often sporadic but rarely can be associated with Pallister-Hall syndrome, an autosomal dominant familial syndrome caused by truncation of glioblastoma transcription factor 3, a downstream effector in the sonic hedgehog pathway. In this clinical report, the authors describe two brothers with a different familial syndrome. To the best of the authors' knowledge, this is the first report in the literature describing a familial syndrome caused by germline mutations in the Smoothened (SMO) gene and the first familial syndrome associated with hypothalamic hamartomas other than Pallister-Hall syndrome. The authors discuss the endoscopic endonasal biopsy and subtotal resection of a large hypothalamic hamartoma in one of the patients as well as the histopathological findings encountered. Integral to this discussion is the understanding of the hedgehog pathway; therefore, the underpinnings of this pathway and its clinical associations to date are also reviewed.

Entities:  

Keywords:  Chiari malformation type I; DI = diabetes insipidus; Dhh = desert hedgehog; GFAP = glial fibrillary acidic protein; GLI = glioblastoma transcription factor; GRK2 = G protein–coupled receptor kinase 2; Hh = hedgehog; Ihh = Indian hedgehog; PTCH = Patched; SMO; SUFU = Suppressor of Fused; Shh = sonic hedgehog; Smoothened gene; gelastic/dacrystic seizures; hypothalamic hamartoma; oncology

Mesh:

Substances:

Year:  2018        PMID: 30497210     DOI: 10.3171/2018.7.PEDS18292

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  6 in total

1.  Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndrome.

Authors:  Michael S Hildebrand; Samuel F Berkovic; Timothy E Green; Mareike Schimmel; Susanna Schubert; Johannes R Lemke; Mark F Bennett
Journal:  Eur J Hum Genet       Date:  2022-01-16       Impact factor: 4.246

2.  Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO).

Authors:  Lihong Fan; Pengzhen Jin; Yeqing Qian; Guosong Shen; Xueping Shen; Minyue Dong
Journal:  Front Genet       Date:  2022-06-22       Impact factor: 4.772

3.  Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

Authors:  Timothy E Green; Joshua E Motelow; Mark F Bennett; Zimeng Ye; Caitlin A Bennett; Nicole G Griffin; John A Damiano; Richard J Leventer; Jeremy L Freeman; A Simon Harvey; Paul J Lockhart; Lynette G Sadleir; Amber Boys; Ingrid E Scheffer; Heather Major; Benjamin W Darbro; Melanie Bahlo; David B Goldstein; John F Kerrigan; Erin L Heinzen; Samuel F Berkovic; Michael S Hildebrand
Journal:  Hum Mol Genet       Date:  2022-07-21       Impact factor: 5.121

4.  Sonic Hedgehog repression underlies gigaxonin mutation-induced motor deficits in giant axonal neuropathy.

Authors:  Yoan Arribat; Karolina S Mysiak; Léa Lescouzères; Alexia Boizot; Maxime Ruiz; Mireille Rossel; Pascale Bomont
Journal:  J Clin Invest       Date:  2019-12-02       Impact factor: 14.808

5.  Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling.

Authors:  Thuy-Linh Le; Yunia Sribudiani; Xiaomin Dong; Céline Huber; Chelsea Kois; Geneviève Baujat; Christopher T Gordon; Valerie Mayne; Louise Galmiche; Valérie Serre; Nicolas Goudin; Mohammed Zarhrate; Christine Bole-Feysot; Cécile Masson; Patrick Nitschké; Frans W Verheijen; Lynn Pais; Anna Pelet; Simon Sadedin; John A Pugh; Natasha Shur; Susan M White; Salima El Chehadeh; John Christodoulou; Valérie Cormier-Daire; R M W Hofstra; Stanislas Lyonnet; Tiong Yang Tan; Tania Attié-Bitach; Wilhelmina S Kerstjens-Frederikse; Jeanne Amiel; Sophie Thomas
Journal:  Am J Hum Genet       Date:  2020-05-14       Impact factor: 11.025

Review 6.  Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal Phenotypes.

Authors:  Yo Niida; Sumihito Togi; Hiroki Ura
Journal:  Int J Mol Sci       Date:  2021-12-02       Impact factor: 5.923

  6 in total

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