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

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.
AuthorsSebastian Rubino, Jiang Qian, Carlos D Pinheiro-Neto, Tyler J Kenning, Matthew A Adamo
JournalJournal of neurosurgery. Pediatrics (J Neurosurg Pediatr) Vol. 23 Issue 1 Pg. 98-103 (10 12 2018) ISSN: 1933-0715 [Electronic] United States
PMID30497210 (Publication Type: Case Reports, Journal Article)
Chemical References
  • GLI3 protein, human
  • Nerve Tissue Proteins
  • SMO protein, human
  • Smoothened Receptor
  • Zinc Finger Protein Gli3
Topics
  • Child
  • Child, Preschool
  • Germ-Line Mutation (genetics)
  • Hamartoma (complications, diagnostic imaging, genetics, surgery)
  • Humans
  • Hypothalamic Diseases (complications, diagnostic imaging, genetics, surgery)
  • Magnetic Resonance Imaging
  • Male
  • Nerve Tissue Proteins (genetics)
  • Polydactyly (complications, genetics)
  • Siblings
  • Smoothened Receptor (genetics)
  • Syndrome
  • Zinc Finger Protein Gli3 (genetics)

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