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Frontometaphyseal dysplasia: neonatal radiographic diagnosis.
Am J Med Genet. 1995 May 22; 57(1):1-5.AJ

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.

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Authors+Show Affiliations

Glass RB
Department of Diagnostic Imaging and Radiology, Children's National Medical Center, Washington, District of Columbia, USA.
Rosenbaum KN
No affiliation info available

MeSH

Abnormalities, MultipleAdultChild, PreschoolConnective TissueFacial BonesFemaleHumansInfant, NewbornMaleRadiographySkull

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

7645585

Citation

Glass, R B., and K N. Rosenbaum. "Frontometaphyseal Dysplasia: Neonatal Radiographic Diagnosis." American Journal of Medical Genetics, vol. 57, no. 1, 1995, pp. 1-5.
Glass RB, Rosenbaum KN. Frontometaphyseal dysplasia: neonatal radiographic diagnosis. Am J Med Genet. 1995;57(1):1-5.
Glass, R. B., & Rosenbaum, K. N. (1995). Frontometaphyseal dysplasia: neonatal radiographic diagnosis. American Journal of Medical Genetics, 57(1), 1-5.
Glass RB, Rosenbaum KN. Frontometaphyseal Dysplasia: Neonatal Radiographic Diagnosis. Am J Med Genet. 1995 May 22;57(1):1-5. PubMed PMID: 7645585.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Frontometaphyseal dysplasia: neonatal radiographic diagnosis. AU - Glass,R B, AU - Rosenbaum,K N, PY - 1995/5/22/pubmed PY - 1995/5/22/medline PY - 1995/5/22/entrez SP - 1 EP - 5 JF - American journal of medical genetics JO - Am J Med Genet VL - 57 IS - 1 N2 - 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. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/7645585/Frontometaphyseal_dysplasia:_neonatal_radiographic_diagnosis_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1995&volume=57&issue=1&spage=1 DB - PRIME DP - Unbound Medicine ER -