Autosomal dominantly inherited adductor laryngeal paralysis--a new syndrome with a suggestion of linkage to HLA.

Clinical genetics ·Vol. 14 ·No. 5 ·1978-11-00 ·Pages 265-70

Mace M, Williamson E, Worgan D

Abstract

A family is reported with autosomal dominantly inherited congenital bilateral adductor paralysis of the larynx. This disorder has apparently not been described previously. A search for linkage in this family with the loci for 19 other genetic markers showed a suggestion of linkage with HLA and GLO, and accordingly a suggestion that the locus for this disorder may be assigned to chromosome 6.

MeSH Terms

Adolescent Aged Child Child, Preschool Chromosomes, Human, 6-12 and X Female Genes, Dominant Genetic Linkage Glyoxylates HLA Antigens Humans Male Pedigree Syndrome Vocal Cord Paralysis/genetics

Chemicals

Glyoxylates HLA Antigens

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Mace M

Williamson E

Worgan D

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

DOI

10.1111/j.1399-0004.1978.tb02145.x

Published

1978-11-00

Pages

265-70

Language

English

Region

Denmark

NLM ID

0253664

Subset

External Links

PubMed source DOI: 10.1111/j.1399-0004.1978.tb02145.x View journal details

Analysis Services

Autosomal dominantly inherited adductor laryngeal paralysis--a new syndrome with a suggestion of linkage to HLA.

Contact

WeChat Official Account