A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies

Am J Med Genet A. 2023 Jan;191(1):100-107. doi: 10.1002/ajmg.a.62994. Epub 2022 Oct 29.

Abstract

We present a large, ten-generation family of 273 individuals with 84 people having preaxial polydactyly/triphalangeal thumb due to a pathogenic variant in the zone of polarizing activity regulatory sequence (ZRS) within the exon 5 of LMBR1. The causative change maps to position 396 of the ZRS, located at position c.423 + 4909C > T (chr7:156791480; hg38; LMBR1 ENST00000353442.10; rs606231153 NG_009240.2) in the intron 5 of LMBR1. The first affected individual with the disorder was traced back to mid-1700, when some settlers and workers established in Cervera de Buitrago, a small village about 82 km North to Madrid. Clinical and radiological studies of most of the affected members have been performed for 42 years (follow-up of the family by LFGA). Molecular studies have confirmed a pathogenic variant in the ZRS that segregates in this family. To the best of our knowledge, this is the largest family with preaxial polydactyly/triphalangeal thumb reported so far.

Keywords: ZRS; intron 5 of LMBR1; polarizing activity regulatory sequence; preaxial polydactyly; semidominant inheritance; triphalangeal thumb.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Membrane Proteins* / genetics
  • Pedigree
  • Polydactyly* / genetics
  • Polydactyly* / pathology
  • Thumb / pathology

Substances

  • Membrane Proteins

Supplementary concepts

  • Polydactyly preaxial type 1
  • Triphalangeal Thumb