Suspect dyskeratotic neoformations in a 7-year-old child with keratitis-ichthyosis-deafness syndrome: diagnostic, surgical and wound care management
Keratitis-ichthyosis-deafness syndrome (KID) is a rare genetic disorder characterized by the triad of hyperkeratosis, ichthyosis, and congenital prelingual sensorineural deafness, with less than 100 cases described in the literature. In addition to many other extra-cutaneous manifestations, these p...
Main Authors: | Alvise Montanari, Francesca Caroppo, Antonio Amabile, Anna Fortina Belloni, Franco Bassetto |
---|---|
Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2024-04-01
|
Series: | Dermatology Reports |
Subjects: | |
Online Access: | https://www.pagepress.org/journals/dr/article/view/9953 |
Similar Items
-
Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa
by: Lisa Travis, MD, et al.
Published: (2023-08-01) -
Large intraoral Lipoma: A case report of rare neoformation of the lower lip
by: Paola Bonavolontà, et al.
Published: (2023-03-01) -
Isolation and Identification of Cryptococcus neoformans from Human Skin Lesions and Application of Animal Experiment (in vivo)
by: Mahmood F. A.
Published: (2015-06-01) -
Ultrasonic Patterns of Benign Skin Formations
by: M. A. Bizunova, et al.
Published: (2018-02-01) -
Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients
by: Kalezić T, et al.
Published: (2023-03-01)