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[Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family].
Z Orthop Ihre Grenzgeb. 1988 Jan-Feb; 126(1):34-8.ZO

Abstract

The trichorhinophalangeal syndrome type I is a rare, probably autosomal-dominant inherited disorder, characterized by anomalies of the cranium and face, hair, skeleton and soft parts of the hands and the feet. Typical deformities of the syndrome in hands and feet (e.g. brachydactylie, deviation and curvature of fingers and toes due to cone-shaped joints) are explained by description of the findings in three adult members of a family.

Authors+Show Affiliations

Unfallchirurgische Klinik des Friederikenstiftes Hannover.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

ger

PubMed ID

3381568

Citation

Meyer, H H., et al. "[Hand and Foot Deformities in a Type I Trichorhinophalangeal Syndrome. Studies in 3 Members of a Family]." Zeitschrift Fur Orthopadie Und Ihre Grenzgebiete, vol. 126, no. 1, 1988, pp. 34-8.
Meyer HH, Prescher W, Reime J. [Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family]. Z Orthop Ihre Grenzgeb. 1988;126(1):34-8.
Meyer, H. H., Prescher, W., & Reime, J. (1988). [Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family]. Zeitschrift Fur Orthopadie Und Ihre Grenzgebiete, 126(1), 34-8.
Meyer HH, Prescher W, Reime J. [Hand and Foot Deformities in a Type I Trichorhinophalangeal Syndrome. Studies in 3 Members of a Family]. Z Orthop Ihre Grenzgeb. 1988 Jan-Feb;126(1):34-8. PubMed PMID: 3381568.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family]. AU - Meyer,H H, AU - Prescher,W, AU - Reime,J, PY - 1988/1/1/pubmed PY - 1988/1/1/medline PY - 1988/1/1/entrez SP - 34 EP - 8 JF - Zeitschrift fur Orthopadie und ihre Grenzgebiete JO - Z Orthop Ihre Grenzgeb VL - 126 IS - 1 N2 - The trichorhinophalangeal syndrome type I is a rare, probably autosomal-dominant inherited disorder, characterized by anomalies of the cranium and face, hair, skeleton and soft parts of the hands and the feet. Typical deformities of the syndrome in hands and feet (e.g. brachydactylie, deviation and curvature of fingers and toes due to cone-shaped joints) are explained by description of the findings in three adult members of a family. SN - 0044-3220 UR - https://www.unboundmedicine.com/medline/citation/3381568/[Hand_and_foot_deformities_in_a_type_I_trichorhinophalangeal_syndrome__Studies_in_3_members_of_a_family]_ L2 - http://www.thieme-connect.com/DOI/DOI?10.1055/s-2008-1044864 DB - PRIME DP - Unbound Medicine ER -