Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy Syndrome

Alternative Names

  • EEMS
  • EEM Syndrome

Associated Genes

Cadherin 3
Back to search Result
WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Other congenital malformations

OMIM Number

225280

Mode of Inheritance

Autosomal recessive

Gene Map Locus

16q22.1

Description

EEM syndrome denotes a disorder characterized by ectodermal dysplasia, ectrodactyly, and macular dystrophy. The ectodermal dysplasia consists of hypotrichosis affecting scalp hair, eyebrows, and eyelashes, with partial anodontia. Different degrees of absence deformities as well as syndactyly have been described, the hands often being more severely affected than the feet. The retinal lesion appears as a central geographic atrophy of the retinal pigment epithelium and choriocapillary layer of the macular area with coarse hyperpigmentations and sparing of the larger choroidal vessels. [From OMIM]

Epidemiology in the Arab World

View Map
Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
225280.1.1Saudi ArabiaMaleYesYes Ectrodactyly; Macular dystrophyNM_001793.6:c.1182+1G>AHomozygousAutosomal, RecessiveMaddirevula et al. 2018
225280.1.2Saudi ArabiaMaleYesYes Ectrodactyly; Macular dystrophyNM_001793.6:c.1182+1G>AHomozygousAutosomal, RecessiveMaddirevula et al. 2018 Relative of 225280.1...
225280.2.1Saudi ArabiaMaleYesYes Rod-cone dystrophy; Abnormal facial shap...NM_001793.6:c.307C>THomozygousAutosomal, RecessiveMaddirevula et al. 2018
225280.2.2Saudi ArabiaMaleYesYes Rod-cone dystrophy; Abnormal facial shap...NM_001793.6:c.307C>THomozygousAutosomal, RecessiveMaddirevula et al. 2018 Relative of 225280.2...
© CAGS 2024. All rights reserved.