Yasaan Saaqib, Nabeela Shahzadi, Zahid Tahir, Nadia Ali Azfar.
Clinical Diagnosis of Kindler Syndrome: a Report of Two Cases from a District Hospital in Gujranwala, Pakistan.
J Pak Assoc Derma Jan ;33(3):1106-11.

 Kindler syndrome is a rare autosomal recessive disorder belonging to the group of Epidermolysis Bullosa (EB), which encompasses genetic disorders affecting the skin and mucous membranes. This case report aims to contribute to the limited literature on Kindler syndrome by presenting two cases observed at a district hospital in Gujranwala, Pakistan. The cases involve a brother and sister displaying typical symptoms and having a family history of the disease. The objective is to enhance clinicians' awareness of this rare disorder and emphasize the significance of clinical diagnosis-driven management strategies.

PakMediNet -Pakistan's largest Database of Pakistani Medical Journals - http://www.pakmedinet.com