Lacrimal Gland Involvement in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome

Ophthalmology. 2017 Mar;124(3):399-406. doi: 10.1016/j.ophtha.2016.10.028. Epub 2016 Nov 30.

Abstract

Purpose: To describe the involvement of the lacrimal gland (LG) in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).

Design: Observational, cross-sectional study.

Participants: Twenty-one patients with BPES (10 female, 11 male) aged on average 15 years (range, 2-39 years), from 3 Brazilian medical centers and 1 Portuguese medical center.

Methods: Patients had their ocular surface evaluated with slit-lamp biomicroscopy, and tear production quantified with the Schirmer test I. The LG volumes were measured on computed tomography (CT) scans in the BPES sample and in a group of age-matched subjects imaged for nonorbital diseases. Sixteen patients were screened for mutations in the FOXL2 gene.

Main outcome measures: Lacrimal meniscus height, Schirmer test I, presence of superficial punctate keratopathy (SPK), LG volume, and molecular analysis of the FOXL2 gene.

Results: Absence of LG was detected bilaterally in 9 patients (42.8%) and unilaterally in 2 patients (9.5%). When considering only patients with measurable LG, the median volume was 0.22 cm3 in the right eye (range, 0.06-0.36 cm3) and 0.24 cm3 in the left eye (range, 0.08-0.34 cm3). These values were significantly lower than those for the age-matched controls (median = 0.54 right eye and 0.53 left eye; P < 0.05). There was a significant association between deficiency of tear production and LG volume reduction and agenesis. Molecular analysis of the FOXL2 gene revealed the presence of 8 distinct mutations, 4 of them novel ones. A significant reduction of LG size or agenesis was associated with mutations affecting protein size (due to underlying changes in the stop codon location) or the DNA-binding forkhead domain (Fisher exact test, P = 0.021). In 3 probands, the underlying genetic defect was not found.

Conclusions: This is the first study reporting LG volumes in BPES, describing a significant number of patients with LG agenesis. The association between alacrima and BPES is not incidental, and a thorough evaluation of tear production is recommended especially if ptosis surgery is planned.

Publication types

  • Observational Study

MeSH terms

  • Adolescent
  • Adult
  • Blepharophimosis / diagnostic imaging*
  • Blepharophimosis / genetics
  • Child
  • Child, Preschool
  • Cross-Sectional Studies
  • DNA Mutational Analysis
  • Exons / genetics
  • Eye Abnormalities / diagnostic imaging*
  • Eye Abnormalities / genetics
  • Female
  • Forkhead Box Protein L2
  • Forkhead Transcription Factors / genetics*
  • Gene Amplification
  • Genetic Association Studies
  • Humans
  • Lacrimal Apparatus / abnormalities*
  • Male
  • Skin Abnormalities / diagnostic imaging*
  • Skin Abnormalities / genetics
  • Slit Lamp Microscopy
  • Tears / physiology
  • Tomography, X-Ray Computed*
  • Urogenital Abnormalities / diagnostic imaging*
  • Urogenital Abnormalities / genetics

Substances

  • FOXL2 protein, human
  • Forkhead Box Protein L2
  • Forkhead Transcription Factors

Supplementary concepts

  • Blepharophimosis, Ptosis, and Epicanthus Inversus