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 pa...
Saved in:
Main Authors: | Alvise Montanari (Author), Francesca Caroppo (Author), Antonio Amabile (Author), Anna Fortina Belloni (Author), Franco Bassetto (Author) |
---|---|
Format: | Book |
Published: |
PAGEPress Publications,
2024-04-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa
by: Lisa Travis, MD, et al.
Published: (2023) -
Keratitis-Ichthyosis-Deafness (KID) Syndrome, case report
by: Tomasz Wasyłyszyn, et al.
Published: (2017) -
Keratitis-Ichthyosis-Deafness syndrome: A rare congenital disorder
by: Vinay Shanker, et al.
Published: (2012) -
Keratitis-Ichthyosis-Deafness: A rare kid in clinical practice
by: Shikha R Shah, et al.
Published: (2022) -
Clinical Observation of a Child with KID (Keratitis-Ichthyosis-Deafness) Syndrome
by: V.A. Klymenko, et al.
Published: (2015)