EC Clinical and Medical Case Reports

Case Report Volume 6 Issue 2 - 2023

Ophthalmological Manifestations in a Patient with Hypohidrotic Ectodermal Dysplasia

Samuel Josue Avalos Lara1*, Oscar Baca Lozada1, Oscar Fernández Vizcaya1, Lorenza Céspedes Pastrana2, Cristina Mendoza Velásquez3 and Josefina de Peña Ortíz4

1Department of Cornea and Refractive Surgery, Fundación Hospital Nuestra Señora de la Luz, I.A.P, Mexico City, Mexico

2Department of Glaucoma, Fundación Hospital Nuestra Señora de la Luz, I.A.P, Mexico City, Mexico

3Department of Anterior Segment, Fundación Hospital Nuestra Señora de la Luz, I.A.P, Mexico City, Mexico

4Dermatology, Centro Dermatológico Dr. Ladislao de la Pascua, Mexico City, Mexico

*Corresponding Author: Samuel Josue Avalos Lara, Department of Cornea and Refractive Surgery, Fundación Hospital Nuestra Señora de la Luz, I.A.P, Mexico City, Mexico.
Received: December 15, 2022; Published: January 31, 2023



Hypohidrotic ectodermal dysplasia is a rare genetic disorder characterized by defective development of the ectodermal structure, resulting in anhidrosis/hypo hidrosis, hypotrichosis, and hypodontia. This condition is usually an X-linked recessive disorder that predominantly affects males. Various ophthalmological manifestations have been reported in the literature. We present the ophthalmological manifestations in a case of hypo hidrotic ectodermal dysplasia.

Keywords: Hypohidrotic Ectodermal Dysplasia; Hypotrichosis; Hypodontia

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Samuel Josue Avalos Lara et al. Ophthalmological Manifestations in a Patient with Hypohidrotic Ectodermal Dysplasia. EC Clinical and Medical Case Reports   6.2 (2023): 78-83.