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Frontometaphyseal dysplasia: Neonatal radiographic diagnosis

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Glass, Ronald B. J., Rosenbaum, Kenneth N.·1995·American Journal of Medical Genetics

Abstract

Frontometaphyseal dysplasia (FMD) is an uncommon genetic syndrome affecting bone and connective tissue. This condition is characterized by hyperostosis of the skull and prominence of the supraorbital ridges; long bones have flared metaphyses. Frontometaphyseal dysplasia is an X‐linked dominant trait with more severe manifestations in males and with extreme variability in females. Diagnosis in the neonatal period is difficult. We present 2 newborn boys with the radiographic findings of FMD. © 1995 Wiley‐Liss, Inc.

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Metadata

Authors
Glass, R. B. J., & Rosenbaum, K. N.
Venue
American Journal of Medical Genetics
Publisher
Wiley
Published
1995-05-22
Volume
57
Issue
1
Pages
1-5
ISSN
  • 0148-7299 (ISSN-L)
  • 1096-8628
OpenAlex
W1526977350
Cited by
189
References
0
FWCI
16.83
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Frontometaphyseal dysplasia: Neonatal radiographic diagnosis. https://app.cochat.ai/papers/10.1002/ajmg.1320570102
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Glass, R. B. J., & Rosenbaum, K. N. (1995). Frontometaphyseal dysplasia: Neonatal radiographic diagnosis. American Journal of Medical Genetics. https://doi.org/10.1002/ajmg.1320570102

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