Literature DB >> 925743

Genetic perspectives on craniosynostosis and syndromes with craniosynostosis.

M M Cohen.   

Abstract

Thirty-seven syndromes in which craniosynostosis is a feature are presented in tabular form, allowing the clinician to rapidly identify a given syndrome and gain immediate access to the pertinent literature. A plea is made to delineate unknown genesis syndromes with craniosynostosis as rapidly as possible. As an unknown genesis syndrome becomes delineated, its phenotypic spectru, its natural history, and its inheritance pattern or risk of recurrence become known, allowing for better patient care and family counseling.

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Year:  1977        PMID: 925743     DOI: 10.3171/jns.1977.47.6.0886

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  6 in total

1.  CT findings in complete premature craniosynostosis.

Authors:  J R Jinkins
Journal:  Neuroradiology       Date:  1987       Impact factor: 2.804

2.  Osteoglophonic dwarfism in two generations.

Authors:  R I Kelley; P F Borns; D Nichols; E H Zackai
Journal:  J Med Genet       Date:  1983-12       Impact factor: 6.318

3.  Craniosynostosis and Craniofacial Anomalies.

Authors: 
Journal:  West J Med       Date:  1980-06

4.  Perspectives on Craniosynostosis.

Authors:  M M Cohen
Journal:  West J Med       Date:  1980-06

5.  Premature craniosynostosis. A retrospective analysis of a series of 52 cases.

Authors:  M Bernardy; E Donauer; D Neuenfeldt
Journal:  Acta Neurochir (Wien)       Date:  1994       Impact factor: 2.216

6.  A family study of craniosynostosis, with probable recognition of a distinct syndrome.

Authors:  C O Carter; K Till; V Fraser; R Coffey
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

  6 in total

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