<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>Primary defects in two or more ectodermally-derived tissues during embryonic development characterize ectodermal dysplasia, a vast, varied group of inherited illnesses. Skin, hair, nails, eccrine glands, and teeth are the primary tissues affected. Most cases of ectodermal dysplasia are caused by the X-linked recessive form of the disease (also known as Christ–Siemens–Touraine syndrome), which is passed down from female carriers to their male offspring. It is characterized by an absence of sweat glands (hypohidrosis or anhidrosis), malformed teeth (anodontia or hypodontia), and scant hair (atrichosis or hypotrichosis). Lack of teeth and unusual look were cited as major causes for alarm. The usual manifestations of hypohidrotic hereditary ectodermal dysplasia have been described in two case reports. Two identical siblings with possible typically X-linked recessive hypohidrotic ectodermal dysplasia are described here. Despite the lack of a cure, patients can benefit from a multidisciplinary approach to treatment planning and an expedient diagnosis.</p>
</abstract>

Primary defects in two or more ectodermally-derived tissues during embryonic development characterize ectodermal dysplasia, a vast, varied group of inherited illnesses. Skin, hair, nails, eccrine glands, and teeth are the primary tissues affected. Most cases of ectodermal dysplasia are caused by the X-linked recessive form of the disease (also known as Christ–Siemens–Touraine syndrome), which is passed down from female carriers to their male offspring. It is characterized by an absence of sweat glands (hypohidrosis or anhidrosis), malformed teeth (anodontia or hypodontia), and scant hair (atrichosis or hypotrichosis). Lack of teeth and unusual look were cited as major causes for alarm. The usual manifestations of hypohidrotic hereditary ectodermal dysplasia have been described in two case reports. Two identical siblings with possible typically X-linked recessive hypohidrotic ectodermal dysplasia are described here. Despite the lack of a cure, patients can benefit from a multidisciplinary approach to treatment planning and an expedient diagnosis.

Hereditary Ectodermal Dysplasia in Two Identical Siblings

Nitte (Deemed to be University), AB Shetty Memorial Institute of Dental Sciences (ABSMIDS)

Department of Oral Medicine and Radiology

Acta Medica Bulgarica

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

{"article-title":"Hereditary Ectodermal Dysplasia in Two Identical Siblings"}

Primary defects in two or more ectodermally-derived tissues during embryonic development characterize ectodermal dysplasia, a vast, varied group of inherited...

Hereditary Ectodermal Dysplasia in Two Identical Siblings

Publié en ligne: 29 juin 2024

Pages: 1 - 4

Reçu: 07 juin 2023

Accepté: 04 avr. 2024

DOI: https://doi.org/10.2478/amb-2024-0023

Mots clés
anodontia, consanguineous siblings, hereditary disease, hypotrichosis, hypohidrosis

© 2024 A. S. Sarkar et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Hereditary Ectodermal Dysplasia in Two Identical Siblings

Publié en ligne: 29 juin 2024

Pages: 1 - 4

Reçu: 07 juin 2023

Accepté: 04 avr. 2024

DOI: https://doi.org/10.2478/amb-2024-0023

Mots clésanodontia, consanguineous siblings, hereditary disease, hypotrichosis, hypohidrosis

© 2024 A. S. Sarkar et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Mots clés
anodontia, consanguineous siblings, hereditary disease, hypotrichosis, hypohidrosis