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A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).
Acta Paediatr Scand. 1981 Mar; 70(2):275-7.AP

Abstract

A newborn infant with craniofacial dysmorphism and polysndactyly (Greig's Syndrome) is reported. This syndrome is manifested by postaxial polydactyly of the fingers and preaxial polydactyly of the toes, with syndactyly. The craniofacial dysmorphism is characterized by frontal bossing and other variable manifestations. X-ray examination revealed markedly advanced bone age. The mode of inheritance appears to be autosomal dominant.

Authors

Merlob P
No affiliation info available
Grünebaum M
No affiliation info available
Reisner SH
No affiliation info available

MeSH

Abnormalities, MultipleBone DevelopmentFacial BonesFemaleFingersHumansInfant, NewbornSkullSyndactylySyndromeToes

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

6263040

Citation

Merlob, P, et al. "A Newborn Infant With Craniofacial Dysmorphism and Polysyndactyly (Greig's Syndrome)." Acta Paediatrica Scandinavica, vol. 70, no. 2, 1981, pp. 275-7.
Merlob P, Grünebaum M, Reisner SH. A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome). Acta Paediatr Scand. 1981;70(2):275-7.
Merlob, P., Grünebaum, M., & Reisner, S. H. (1981). A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome). Acta Paediatrica Scandinavica, 70(2), 275-7.
Merlob P, Grünebaum M, Reisner SH. A Newborn Infant With Craniofacial Dysmorphism and Polysyndactyly (Greig's Syndrome). Acta Paediatr Scand. 1981;70(2):275-7. PubMed PMID: 6263040.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome). AU - Merlob,P, AU - Grünebaum,M, AU - Reisner,S H, PY - 1981/3/1/pubmed PY - 1981/3/1/medline PY - 1981/3/1/entrez SP - 275 EP - 7 JF - Acta paediatrica Scandinavica JO - Acta Paediatr Scand VL - 70 IS - 2 N2 - A newborn infant with craniofacial dysmorphism and polysndactyly (Greig's Syndrome) is reported. This syndrome is manifested by postaxial polydactyly of the fingers and preaxial polydactyly of the toes, with syndactyly. The craniofacial dysmorphism is characterized by frontal bossing and other variable manifestations. X-ray examination revealed markedly advanced bone age. The mode of inheritance appears to be autosomal dominant. SN - 0001-656X UR - https://www.unboundmedicine.com/medline/citation/6263040/A_newborn_infant_with_craniofacial_dysmorphism_and_polysyndactyly__Greig's_syndrome__ L2 - http://www.diseaseinfosearch.org/result/5854 DB - PRIME DP - Unbound Medicine ER -