Can Hutchinson-Gilford progeria syndrome be a neonatal condition?

Am J Med Genet. 1999 Dec 22;87(5):450-2; author reply 453-4. doi: 10.1002/(sici)1096-8628(19991222)87:5<450::aid-ajmg16>3.0.co;2-t.

Authors

L Faivre, P Khau Van Kien, N Madinier-Chappat, A Nivelon-Chevallier, F Beer, M LeMerrer

PMID: 10594888
DOI: 10.1002/(sici)1096-8628(19991222)87:5<450::aid-ajmg16>3.0.co;2-t

No abstract available

Publication types

Case Reports
Letter
Comment

MeSH terms

Abnormalities, Multiple / diagnosis*
Diagnosis, Differential
Female
Foot Deformities, Congenital / diagnostic imaging
Hand Deformities, Congenital / diagnostic imaging
Humans
Infant
Progeria / diagnosis*
Radiography