Tags

Type your tag names separated by a space and hit enter

[Familial syndrome with lip fistulas and microforms of cleft velum].
Dtsch Zahnarztl Z. 1977 May; 32(5):413-7.DZ

Abstract

Four siblings are reported who have congenital fistulae of their lower lips (with one exception) associated with bifid uvula and partial manifestations of submucous cleft palate, while their mother has a bilateral cleft lip and palate as well as bilateral fistulae of the lip. The malformation is possibly transmitted as an autosomal dominant trait. This special type of hereditary combination is not mentioned in the literature, as far as we know, and appears to be a very rare clinical variation of the syndrome normally associated with clefts of lip and palate and fistulae of the lip.

Authors

Hardt N
No affiliation info available

MeSH

AdolescentAdultChildChild, PreschoolCleft LipCleft PalateFemaleHumansMaleOroantral FistulaPedigreeSyndromeUvula

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

ger

PubMed ID

266463

Citation

Hardt, N. "[Familial Syndrome With Lip Fistulas and Microforms of Cleft Velum]." Deutsche Zahnarztliche Zeitschrift, vol. 32, no. 5, 1977, pp. 413-7.
Hardt N. [Familial syndrome with lip fistulas and microforms of cleft velum]. Dtsch Zahnarztl Z. 1977;32(5):413-7.
Hardt, N. (1977). [Familial syndrome with lip fistulas and microforms of cleft velum]. Deutsche Zahnarztliche Zeitschrift, 32(5), 413-7.
Hardt N. [Familial Syndrome With Lip Fistulas and Microforms of Cleft Velum]. Dtsch Zahnarztl Z. 1977;32(5):413-7. PubMed PMID: 266463.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Familial syndrome with lip fistulas and microforms of cleft velum]. A1 - Hardt,N, PY - 1977/5/1/pubmed PY - 1977/5/1/medline PY - 1977/5/1/entrez SP - 413 EP - 7 JF - Deutsche zahnarztliche Zeitschrift JO - Dtsch Zahnarztl Z VL - 32 IS - 5 N2 - Four siblings are reported who have congenital fistulae of their lower lips (with one exception) associated with bifid uvula and partial manifestations of submucous cleft palate, while their mother has a bilateral cleft lip and palate as well as bilateral fistulae of the lip. The malformation is possibly transmitted as an autosomal dominant trait. This special type of hereditary combination is not mentioned in the literature, as far as we know, and appears to be a very rare clinical variation of the syndrome normally associated with clefts of lip and palate and fistulae of the lip. SN - 0012-1029 UR - https://www.unboundmedicine.com/medline/citation/266463/[Familial_syndrome_with_lip_fistulas_and_microforms_of_cleft_velum]_ DB - PRIME DP - Unbound Medicine ER -