» Articles » PMID: 11832761

Heredity of Hypospadias and the Significance of Low Birth Weight

Overview
Journal J Urol
Publisher Wolters Kluwer
Specialty Urology
Date 2002 Feb 8
PMID 11832761
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: We analyzed a large group of patients with hypospadias regarding familial aggregation, phenotype, twin rate and ethnic origin and assessed the correlation of low birth weight with hypospadias.

Materials And Methods: We mailed questionnaires to 2,503 boys operated on for hypospadias in Sweden asking for additional cases of hypospadias in the family, the number of brothers in the nuclear family, and birth weight of the boys with hypospadias and their brothers.

Results: Of the boys 7% reported 1 or more additional family members with hypospadias. The birth weight of the boys with hypospadias was significantly lower (p = 5 x 10-13) than the birth weight of their unaffected brothers. Phenotyping of 676 individuals revealed glandular hypospadias in 53%, penile forms in 39%, penoscrotal or perineal variants in 6% and cleaved prepuce as the only manifestation in 2%. There were 50% more twins than expected compared to the general population and established zygosity in 83% (67% monozygotic, 33% dizygotic). Non-Swedish ethnicity was noted in 22% of the subjects, a third of whom were from Middle Eastern countries.

Conclusions: We present data on heredity, birth weight, phenotype and ethnic origin in a large group of patients with hypospadias. The finding of additional members with hypospadias in 7% of the families supports the concept that genetic factors are involved in the pathogenesis. The strong association with low birth weight may be explained by genetic and environmental factors.

Citing Articles

Hypospadias Associated With Fetal Growth Restriction: A Multicentric Descriptive and Prognostic Cohort Study.

Marquet M, Anselem O, Bouvattier C, Vivanti A, Benachi A, Jouannic J Prenat Diagn. 2024; 44(13):1567-1573.

PMID: 39500807 PMC: 11628206. DOI: 10.1002/pd.6699.


A qualitative content analysis of the experience of living with hypospadias: varying impact on identity and interpersonal relationships.

Phillips L, Dennermalm N, Ortqvist L, Engberg H, Holmdahl G, Fossum M Front Pediatr. 2024; 12:1459561.

PMID: 39268362 PMC: 11390511. DOI: 10.3389/fped.2024.1459561.


Identifying infrequent genetic changes in monozygotic twins afflicted with hypospadias via targeted panel sequencing.

Kim J, Kim K, Han J, Kim D, Kwak C, Choi J Investig Clin Urol. 2024; 65(5):487-493.

PMID: 39249922 PMC: 11390265. DOI: 10.4111/icu.20230416.


Genome-wide methylation analysis in patients with proximal hypospadias - a pilot study and review of the literature.

van Bever Y, Boers R, Bruggenwirth H, van IJcken W, Magielsen F, de Klein A Epigenetics. 2024; 19(1):2392048.

PMID: 39151125 PMC: 11373573. DOI: 10.1080/15592294.2024.2392048.


Identification of a novel candidate HSD3B2 gene variant for familial hypospadias by whole-exome sequencing.

Almaramhy H, Abdul Samad F, Al-Harbi G, Zaytuni D, Imam S, Masoodi T Front Genet. 2023; 14:1106933.

PMID: 37384334 PMC: 10297146. DOI: 10.3389/fgene.2023.1106933.