Related Experiment Video
Updated: Mar 16, 2026

P50 Sensory Gating in Infants
Published on: December 26, 2013
Kindler's Syndrome: A Tale of Two Siblings
Navya Handa1, Dilip Kachhawa1, Vinod Kumar Jain1
1Department of Dermatology, Dr. S. N. Medical College, Jodhpur, Rajasthan, India.
Abstract:
Kindler's syndrome (KS) is a rare inherited skin disease characterized by acral blistering, photosensitivity, progressive poikiloderma, and cutaneous atrophy along with different types of mucosal involvement. We hereby report KS in two siblings. The case is being reported for its rarity and for emphasizing the importance of considering this condition in the differential diagnosis of disorders that may cause blistering, cutaneous atrophy, and/or poikilodermatous skin changes. Besides, the presentation of the disease in two of the members of the same family makes the case even more interesting.
More Related Videos
07:45An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy
Published on: October 21, 2014
10:11Portable Intermodal Preferential Looking IPL: Investigating Language Comprehension in Typically Developing Toddlers and Young Children with Autism
Published on: December 14, 2012
Related Concept Videos
Meiosis I
Conduct Disorder
Karyotyping
Sex-linked Disorders
Autism Spectrum Disorder
These core symptoms manifest differently among individuals, ranging from mild to severe. The disorder's complexity extends beyond its clinical presentation, encompassing a diverse range of biological, cognitive, and sociocultural influences.
Oppositional Defiant Disorder
Diagnostic Criteria and...