A distinct X-linked syndrome involving joint contractures, keloids, large optic cup-to-disc ratio, and renal stones results from a filamin A (FLNA) mutation

Melissa Lah, Tejasvi Niranjan, Sujata Srikanth, Lynda Holloway, Charles E. Schwartz, Tao Wang, David Weaver

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

We further evaluated a previously reported family with an apparently undescribed X-linked syndrome involving joint contractures, keloids, an increased optic cup-to-disc ratio, and renal stones to elucidate the genetic cause. To do this, we obtained medical histories and performed physical examination on 14 individuals in the family, five of whom are affected males and three are obligate carrier females. Linkage analysis was performed on all but one individual and chromosome X-exome sequencing was done on two affected males. The analysis localized the putative gene to Xq27-qter and chromosome X-exome sequencing revealed a mutation in exon 28 (c.4726G>A) of the filamin A (FLNA) gene, predicting that a conserved glycine had been replaced by arginine at amino acid 1576 (p.G1576R). Segregation analysis demonstrated that all known carrier females tested were heterozygous (G/A), all affected males were hemizygous for the mutation (A allele) and all normal males were hemizygous for the normal G allele. The data and the bioinformatic analysis indicate that the G1576R mutation in the FLNA gene is very likely pathogenic in this family. The syndrome affecting the family shares phenotypic overlap with other syndromes caused by FLNA mutations, but appears to be a distinct phenotype, likely representing a unique genetic syndrome.

Original languageEnglish (US)
Pages (from-to)881-890
Number of pages10
JournalAmerican Journal of Medical Genetics, Part A
Volume170
Issue number4
DOIs
StatePublished - Apr 1 2016

Fingerprint

Filamins
Keloid
Contracture
Joints
Exome
Kidney
Mutation
X Chromosome
Alleles
Genes
Computational Biology
Glycine
Physical Examination
Arginine
Exons
Phenotype
Amino Acids

Keywords

  • Contractures
  • Filamin A
  • FLNA
  • Increased optic cup-to-disc ratio
  • Keloids
  • Uric acid renal stones
  • X-linked

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

A distinct X-linked syndrome involving joint contractures, keloids, large optic cup-to-disc ratio, and renal stones results from a filamin A (FLNA) mutation. / Lah, Melissa; Niranjan, Tejasvi; Srikanth, Sujata; Holloway, Lynda; Schwartz, Charles E.; Wang, Tao; Weaver, David.

In: American Journal of Medical Genetics, Part A, Vol. 170, No. 4, 01.04.2016, p. 881-890.

Research output: Contribution to journalArticle

Lah, Melissa ; Niranjan, Tejasvi ; Srikanth, Sujata ; Holloway, Lynda ; Schwartz, Charles E. ; Wang, Tao ; Weaver, David. / A distinct X-linked syndrome involving joint contractures, keloids, large optic cup-to-disc ratio, and renal stones results from a filamin A (FLNA) mutation. In: American Journal of Medical Genetics, Part A. 2016 ; Vol. 170, No. 4. pp. 881-890.
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