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[Mohr's syndrome : type II orofaciodigital syndrome (author's transl)].
Rev Stomatol Chir Maxillofac. 1981; 82(4):234-40.RS

Abstract

Mohr's syndrome consists of an association of three types of malformation : oral, facial, and digital. It is very similar, therefore, to the syndrome of Papillon-Léage and Psaume. Apart from this, precise, constant characteristics can be recognized which identify it as a separate entity. Firstly, the genetic mode of transmission differs. Secondly, clinical signs are dominated by the frequency and severity of the distal lesions, such that bilateral syndactyly of the big toe is a key element in the differential diagnosis.

Authors

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Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

fre

PubMed ID

6269173

Citation

Ajacques, J C.. "[Mohr's Syndrome : Type II Orofaciodigital Syndrome (author's Transl)]." Revue De Stomatologie Et De Chirurgie Maxillo-faciale, vol. 82, no. 4, 1981, pp. 234-40.
Ajacques JC. [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)]. Rev Stomatol Chir Maxillofac. 1981;82(4):234-40.
Ajacques, J. C. (1981). [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)]. Revue De Stomatologie Et De Chirurgie Maxillo-faciale, 82(4), 234-40.
Ajacques JC. [Mohr's Syndrome : Type II Orofaciodigital Syndrome (author's Transl)]. Rev Stomatol Chir Maxillofac. 1981;82(4):234-40. PubMed PMID: 6269173.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)]. A1 - Ajacques,J C, PY - 1981/1/1/pubmed PY - 1981/1/1/medline PY - 1981/1/1/entrez SP - 234 EP - 40 JF - Revue de stomatologie et de chirurgie maxillo-faciale JO - Rev Stomatol Chir Maxillofac VL - 82 IS - 4 N2 - Mohr's syndrome consists of an association of three types of malformation : oral, facial, and digital. It is very similar, therefore, to the syndrome of Papillon-Léage and Psaume. Apart from this, precise, constant characteristics can be recognized which identify it as a separate entity. Firstly, the genetic mode of transmission differs. Secondly, clinical signs are dominated by the frequency and severity of the distal lesions, such that bilateral syndactyly of the big toe is a key element in the differential diagnosis. SN - 0035-1768 UR - https://www.unboundmedicine.com/medline/citation/6269173/[Mohr's_syndrome_:_type_II_orofaciodigital_syndrome__author's_transl_]_ DB - PRIME DP - Unbound Medicine ER -