Postaxial acrofacial dysostosis or Miller syndrome. A case report.Eur J Pediatr. 1989 Feb; 148(5):445-6.EJ
Abstract
A case of postaxial acrofacial dysostosis (Miller syndrome) is presented. This rare syndrome is essentially characterized by a Treacher-Collins-like facial appearance together with absence of the fifth digital ray of all limbs and variable forearm hypoplasia.
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
2920751
Citation
Barbuti, D, et al. "Postaxial Acrofacial Dysostosis or Miller Syndrome. a Case Report." European Journal of Pediatrics, vol. 148, no. 5, 1989, pp. 445-6.
Barbuti D, Orazi C, Reale A, et al. Postaxial acrofacial dysostosis or Miller syndrome. A case report. Eur J Pediatr. 1989;148(5):445-6.
Barbuti, D., Orazi, C., Reale, A., & Paradisi, C. (1989). Postaxial acrofacial dysostosis or Miller syndrome. A case report. European Journal of Pediatrics, 148(5), 445-6.
Barbuti D, et al. Postaxial Acrofacial Dysostosis or Miller Syndrome. a Case Report. Eur J Pediatr. 1989;148(5):445-6. PubMed PMID: 2920751.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Postaxial acrofacial dysostosis or Miller syndrome. A case report.
AU - Barbuti,D,
AU - Orazi,C,
AU - Reale,A,
AU - Paradisi,C,
PY - 1989/2/1/pubmed
PY - 1989/2/1/medline
PY - 1989/2/1/entrez
SP - 445
EP - 6
JF - European journal of pediatrics
JO - Eur J Pediatr
VL - 148
IS - 5
N2 - A case of postaxial acrofacial dysostosis (Miller syndrome) is presented. This rare syndrome is essentially characterized by a Treacher-Collins-like facial appearance together with absence of the fifth digital ray of all limbs and variable forearm hypoplasia.
SN - 0340-6199
UR - https://www.unboundmedicine.com/medline/citation/2920751/Postaxial_acrofacial_dysostosis_or_Miller_syndrome__A_case_report_
L2 - https://www.diseaseinfosearch.org/result/3012
DB - PRIME
DP - Unbound Medicine
ER -
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