Muscle spasms as presenting feature of Nivelon‐Nivelon‐Mabile syndrome. Issue 1 (22nd October 2022)

• Record Type: Journal Article
• Authors: Saini, Neelam; Das Bhowmik, Aneek; Yareeda, Sireesha; Venkatapuram, Vijayasree; Jabeen, Shaik Afshan; Tallapaka, Karthik; Dalal, Ashwin; Aggarwal, Shagun
• Is Part Of: American journal of medical genetics. Volume 191:Issue 1(2023)
• Page Start: 238
• Page End: 248
• Publication Date: 2022-10-22
• Subjects: HHAT -- Hedgehog pathway -- muscle hypertrophy -- muscle spasm -- microcephaly -- short stature; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.63000
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: Hedgehog acyltransferase gene ( HHAT )‐associated Nivelon‐Nivelon‐Mabile syndrome (NNMS) is a rare genetic disorder of multiple system involvement with microcephaly, central nervous system malformations, skeletal dysplasia, and 46, XY sex reversal. Other variable and inconsistent features reported in this disorder are muscle spasms, facial dysmorphism, prenatal onset growth restriction, microphthalmia, and holoprosencephaly. This is the sixth postnatal reported patient with biallelic variants in HHAT gene, who presented with microcephaly, short stature, muscle hypertrophy, muscle spasms, and facial dysmorphism. The most prominent and presenting finding in this patient were muscle hypertrophy and muscle spasms which had a clinical response to phenytoin and acetazolamide treatment. Our report emphasizes the phenotypic variability of NNMS and further reiterates muscle spasms as an important clinical manifestation of this extremely rare condition.