Literature DB >> 11200992

Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism.

J M Graham1, D Krakow, V T Tolo, A K Smith, R S Lachman.   

Abstract

Acrodysostosis is an uncommon skeletal dysplasia associated with nasal hypoplasia, midface deficiency, severe brachydactyly, and varying degrees of hearing loss and mental retardation. Previous publications have suggested that it may be difficult to distinguish acrodystostosis from pseudohypoparathyroidism on clinical grounds, but acrodysostosis does appear to have distinct clinical and radiologic findings. Spinal stenosis is an underappreciated risk in acrodysostosis, despite the reported loss of normal caudal widening of the lumbar interpediculate distance on AP spine radiographs in the original report of this disorder by Robinow et al., with confirmation of these radiographic findings by Butler et al. We report two sporadic cases of acrodysostosis, one of which required decompressive laminectomy for symptomatic spinal stenosis, and review 11 cases of acrodysostosis from 9 families that were submitted to the International Skeletal Dysplasia Registry. The objective of this report is to determine the frequency and severity of spinal stenosis in patients with acrodysostosis and to summarize the clinical and radiographic findings of acrodysostosis in an effort to distinguish acrodysostosis clearly from pseudohypoparathyroidism. The pattern of brachydactyly differs between these two conditions, and varying degrees of spinal stenosis are characteristic of acrodysostosis. Both our index patients with acrodysostosis had normal bioactivity of the alpha subunit of the Gs protein, therefore indicating that acrodysostosis has a different pathogenesis from pseudohypoparathyroidism. Furthermore, single-strand confirmational polymorphism (SSCP) analysis failed to demonstrate any confirmational alterations in the coding exons of the Gs alpha gene. These radiographic and laboratory findings substantiate that acrodysostosis is clinically different from pseudohypoparathyroidism and that it is necessary to follow patients with acrodysostosis for signs of spinal stenosis.

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Year:  2001        PMID: 11200992     DOI: 10.1007/s002470000355

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

1.  Acrodysostosis and craniofacial conodysplasia are two separate bone dysplasias.

Authors:  Andres Giedion
Journal:  Pediatr Radiol       Date:  2002-03

2.  Exome sequencing identifies PDE4D mutations in acrodysostosis.

Authors:  Hane Lee; John M Graham; David L Rimoin; Ralph S Lachman; Pavel Krejci; Stuart W Tompson; Stanley F Nelson; Deborah Krakow; Daniel H Cohn
Journal:  Am J Hum Genet       Date:  2012-03-29       Impact factor: 11.025

3.  Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis.

Authors:  Caroline Michot; Carine Le Goff; Alice Goldenberg; Avinash Abhyankar; Céline Klein; Esther Kinning; Anne-Marie Guerrot; Philippe Flahaut; Alice Duncombe; Genevieve Baujat; Stanislas Lyonnet; Caroline Thalassinos; Patrick Nitschke; Jean-Laurent Casanova; Martine Le Merrer; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2012-03-29       Impact factor: 11.025

Review 4.  Pseudohypoparathyroidism: one gene, several syndromes.

Authors:  O Tafaj; H Jüppner
Journal:  J Endocrinol Invest       Date:  2016-12-19       Impact factor: 4.256

Review 5.  Acrodysostosis syndromes.

Authors:  C Silve; C Le-Stunff; E Motte; Y Gunes; A Linglart; E Clauser
Journal:  Bonekey Rep       Date:  2012-11-21

Review 6.  Brachydactyly E: isolated or as a feature of a syndrome.

Authors:  Arrate Pereda; Intza Garin; Maria Garcia-Barcina; Blanca Gener; Elena Beristain; Ane Miren Ibañez; Guiomar Perez de Nanclares
Journal:  Orphanet J Rare Dis       Date:  2013-09-12       Impact factor: 4.123

7.  What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.

Authors:  Arrate Pereda; Intza Garin; Guiomar Perez de Nanclares
Journal:  BMC Med Genet       Date:  2018-03-02       Impact factor: 2.103

8.  Acrodysostosis and pseudohypoparathyroidism (PHP): adaptation of Japanese patients with a newly proposed classification and expanding the phenotypic spectrum of variants.

Authors:  Nobuo Matsuura; Tadashi Kaname; Norio Niikawa; Yoshihide Ooyama; Osamu Shinohara; Yukifumi Yokota; Shigeyuki Ohtsu; Noriyuki Takubo; Kazuteru Kitsuda; Keiko Shibayama; Fumio Takada; Akemi Koike; Hitomi Sano; Yoshiya Ito; Kenji Ishikura
Journal:  Endocr Connect       Date:  2022-09-22       Impact factor: 3.221

  8 in total

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