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Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia

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CHILDREN-BASEL
卷 9, 期 9, 页码 -

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MDPI
DOI: 10.3390/children9091357

关键词

ectodermal dysplasia; hypohidrotic ectodermal dysplasia; ocular surface disease; meibomian glands; dry eye; ectodysplasin-A

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Ectodermal dysplasias (EDs) are a group of inherited developmental disorders that affect tissues of ectodermal origin. The most common form, hypohidrotic ectodermal dysplasia (HED), is characterized by missing teeth, hair loss, and lack of sweat glands. HED can also cause ocular symptoms, such as eyelash loss, dry eye symptoms, and potential complications like corneal ulceration and glaucoma.
The term ectodermal dysplasias (EDs) describes a heterogeneous group of inherited developmental disorders that affect several tissues of ectodermal origin. The most common form of EDs is hypohidrotic ectodermal dysplasia (HED), which is characterized by hypodontia, hypotrichosis, and partial or total eccrine sweat gland deficiency. HED is estimated to affect at least 1 in 17,000 people worldwide. Patients with HED have characteristic facies with periorbital hyperpigmentation, depressed nasal bridge, malar hypoplasia, and absent or sparse eyebrows and eyelashes. The common ocular features of HED include madarosis, trichiasis, and ocular chronic surface disease due to dry eye syndrome, which manifests clinically with discomfort, photophobia, and redness. Dry eye is common in HED and results from a combination of ocular surface defects: mucus abnormalities (abnormal conjunctival mucinous glands), aqueous tear deficiency (abnormalities in the lacrimal gland) and lipid deficiency (due to the partial or total absence of the meibomian glands; modified sebaceous glands with the tarsal plate). Sight-threatening complications result from ocular surface disease, including corneal ulceration and perforation with subsequent corneal scarring and neovascularization. Rare ocular features have been reported and include bilateral or unilateral congenital cataracts, bilateral glaucoma, chorioretinal atrophy and atresia of the nasolacrimal duct. Recognition of the ocular manifestations of HED is required to perform clinical surveillance, instigate supportive and preventative treatment, and manage ocular complications.

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