Literature DB >> 7837254

Osteocraniostenosis.

A Verloes1, F Narcy, B Grattagliano, A L Delezoide, P Guibaud, J P Schaaps, M Le Merrer, P Maroteaux.   

Abstract

We report a multiple congenital anomalies (MCA) syndrome in three unrelated fetuses consisting of extremely thin, dense, fishbone-like diaphyses, flared metaphyses, mild micromelic dwarfism, brachydactyly, facial dysmorphism, ocular malformations (microphthalmia, aniridia), cloverleaf skull deformity, and splenic hypoplasia. Histopathological investigations showed abnormalities of the metaphyseal cartilage and adjacent diaphyseal ossification, excessive modelling of the metaphyses, and, in one case, dysplasia of the epiphyseal cartilage. We review three previously reported cases. We suggest the name osteocraniostenosis to describe this radiological and clinical disorder, pinpointing its major clinical and radiological features.

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Year:  1994        PMID: 7837254      PMCID: PMC1050124          DOI: 10.1136/jmg.31.10.772

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  Microcephalic osteodysplastic dwarfism (type II-like) in siblings.

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Journal:  Clin Genet       Date:  1987-08       Impact factor: 4.438

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Journal:  J Bone Joint Surg Am       Date:  1988-08       Impact factor: 5.284

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Journal:  Radiology       Date:  1966-01       Impact factor: 11.105

Review 4.  [Lethal syndromes with thin bones].

Authors:  P Maroteaux; L Cohen-Solal; J Bonaventure; M O Peter; C Francannet; P Guibaud; C Moraine
Journal:  Arch Fr Pediatr       Date:  1988 Aug-Sep

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Authors:  G Currarino; J M Friedman
Journal:  Am J Med Genet       Date:  1986-12

6.  Intrauterine dwarfism, peculiar facies and thin bones with multiple fractures--a new syndrome.

Authors:  K Kozlowski; A Kan
Journal:  Pediatr Radiol       Date:  1988

7.  A lethal autosomal recessive syndrome of multiple congenital contractures.

Authors:  R Herva; J Leisti; P Kirkinen; U Seppänen
Journal:  Am J Med Genet       Date:  1985-03
  7 in total
  4 in total

Review 1.  Pansynostosis: a review.

Authors:  Jeffrey P Blount; Robert G Louis; R Shane Tubbs; John H Grant
Journal:  Childs Nerv Syst       Date:  2007-05-08       Impact factor: 1.475

2.  FAM111A mutations result in hypoparathyroidism and impaired skeletal development.

Authors:  Sheila Unger; Maria W Górna; Antony Le Béchec; Sonia Do Vale-Pereira; Maria Francesca Bedeschi; Stefan Geiberger; Giedre Grigelioniene; Eva Horemuzova; Faustina Lalatta; Ekkehart Lausch; Cinzia Magnani; Sheela Nampoothiri; Gen Nishimura; Duccio Petrella; Francisca Rojas-Ringeling; Akari Utsunomiya; Bernhard Zabel; Sylvain Pradervand; Keith Harshman; Belinda Campos-Xavier; Luisa Bonafé; Giulio Superti-Furga; Brian Stevenson; Andrea Superti-Furga
Journal:  Am J Hum Genet       Date:  2013-05-16       Impact factor: 11.025

3.  Case report: targeted whole exome sequencing enables the first prenatal diagnosis of the lethal skeletal dysplasia Osteocraniostenosis.

Authors:  Lara Pemberton; Robert Barker; Anna Cockell; Vijaya Ramachandran; Andrea Haworth; Tessa Homfray
Journal:  BMC Med Genet       Date:  2020-01-07       Impact factor: 2.103

Review 4.  Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features.

Authors:  Simonetta Rosato; Sheila Unger; Belinda Campos-Xavier; Stefano Giuseppe Caraffi; Laura Beltrami; Marzia Pollazzon; Ivan Ivanovski; Marco Castori; Maria Paola Bonasoni; Giuseppina Comitini; Peter G J Nikkels; Kristin Lindstrom; Christine Umandap; Andrea Superti-Furga; Livia Garavelli
Journal:  Genes (Basel)       Date:  2022-01-28       Impact factor: 4.096

  4 in total

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