Infrared meibography and molecular assessment of p63 gene mutations in a Mexican patient with EEC syndrome
Arch Soc Esp Oftalmol (Engl Ed). 2018 Nov;93(11):562-566.
doi: 10.1016/j.oftal.2018.06.005.
Epub 2018 Jul 17.
[Article in
English,
Spanish]
Affiliations
- 1 Departamento de Ciencias Clínicas, División de Ciencias de la Salud, Universidad de Monterrey, San Pedro Garza García, Nuevo León, México; Destellos de Luz IBP, San Pedro Garza García, Nuevo León, México. Electronic address: [email protected].
- 2 Centro de Diagnóstico Molecular y Medicina Personalizada, Departamento de Ciencias Básicas, División de Ciencias de la Salud, Universidad de Monterrey, San Pedro Garza García, Nuevo León, México.
- 3 Biología del desarrollo, Facultad de Medicina, Tecnológico de Monterrey, Monterrey, Nuevo León, México.
Abstract
Objective:
To report the finding of infrared meibography in a Mexican patient with EEC syndrome (Ectrodactyly-ectodermal dysplasia-cleft syndrome) confirmed by molecular analysis of the p63 gene.
Clinical case:
A 31 year-old male patient was seen due to a history of progressive visual loss in both eyes associated with long-term photophobia. The patient was born with cleft lip and palate, ectrodactyly of right hand, and afterwards, displayed nail dysplasia, anodontia and alopecia, with which ectodermal dysplasia was diagnosed. The ophthalmological findings were limited to the adnexa and the ocular surface. In vivo infrared meibography showed total absence of Meibomian glands in the lower eyelids and severe deficiency in the upper eyelids. In addition, it was shown that the patient was a heterozygous carrier of a missense mutation R304W (C → T) in exon 8 of the p63 gene.
Discussion:
The R304W mutation in the p63 gene region is definitely related to characteristics such as the absence of Meibomian glands.
Keywords:
EEC syndrome; Glándulas de Meibomio; Meibografía; Meibography; Meibomian gland; Mutaciones p63; Síndrome EEC; p63 mutations.
Copyright © 2018 Sociedad Española de Oftalmología. Publicado por Elsevier España, S.L.U. All rights reserved.
MeSH terms
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Adult
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Cleft Lip / diagnostic imaging
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Cleft Lip / genetics*
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Cleft Palate / diagnostic imaging
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Cleft Palate / genetics*
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Ectodermal Dysplasia / diagnostic imaging
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Ectodermal Dysplasia / genetics*
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Exons / genetics
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Heterozygote
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Humans
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Infrared Rays
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Male
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Meibomian Glands / abnormalities
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Meibomian Glands / diagnostic imaging*
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Meibomian Glands / pathology
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Mutation, Missense*
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Photophobia / etiology
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Point Mutation*
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Transcription Factors / genetics*
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Transillumination*
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Tumor Suppressor Proteins / genetics*
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Vision Disorders / etiology
Substances
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TP63 protein, human
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Transcription Factors
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Tumor Suppressor Proteins
Supplementary concepts
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Ectrodactyly-cleft lip-palate syndrome