Related Experiment Video
Updated: May 26, 2026

09:37
Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
Published on: August 15, 2019
Sulcus vocalis: evidence for autosomal dominant inheritance
R H G Martins1, T M Gonçalves, D S Neves
1Departamento de Otorrinolaringologia, Faculdade de Medicina de Botucatu, Universidade Estadual de São Paulo Júlio de Mesquita Filho, Botucatu, SP, Brasil.
Genetics and Molecular Research : GMR
|December 24, 2011
Summary
This study suggests sulcus vocalis may be inherited in an autosomal dominant pattern. Evidence from one family across three generations indicates a hereditary basis for this vocal cord condition.
Area of Science:
- Otolaryngology
- Genetics
- Medical Science
Background:
- Sulcus vocalis is a laryngeal condition affecting vocal fold vibration.
- The etiology of sulcus vocalis is not fully understood, with various contributing factors proposed.
Purpose of the Study:
- To investigate the potential hereditary transmission of sulcus vocalis.
- To propose an etiological model for sulcus vocalis based on family pedigree analysis.
Main Methods:
- Clinical examination of four dysphonic patients from three generations of a single family.
- Videolaryngoscopy and direct laryngoscopy were utilized for diagnosis.
Main Results:
- Sulcus vocalis was diagnosed in all four examined patients.
- The affected individuals spanned three generations, demonstrating vertical transmission in both males and females.
Conclusions:
- The observed pattern of inheritance strongly suggests an autosomal dominant mode for sulcus vocalis.
- This family pedigree provides evidence for a genetic basis of sulcus vocalis.
Related Concept Videos
Pedigree Analysis
Overview
Pedigree Analysis
Overview
Pleiotropy
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
X-linked Traits
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
X-linked Traits
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
Sex-linked Disorders
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.

