This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Kindler syndrome

Authoring team

Kindler syndrome is a rare genodermatosis characterized by acral bullae and photosensitivity

  • photosensitivity improves with advancing age and results in progressive poikiloderma and cutaneous atrophy
  • classical features include acral blistering and photosensitivity in childhood, and subsequent development of poikiloderma, leukokeratosis of oro-ano-genital mucosae, phimosis and meatal stenosis
  • additional features noted in two case reports include:
    • in one patient additional ophthalmic features of chronic simple conjunctivitis caused by persistent irritation, multiple stromal nebular corneal opacities and thickened corneal nerves
    • in one patient skeletal changes, namely a dome-shaped skull (turri-cephaly), bifid fourth rib, missing fifth rib, short fourth and fifth metacarpals and mandibular abnormalitie

Reference:

  1. Sharma JC et al. Kindler syndrome. Int J Dermatol. 2003 Sep;42(9):727-32

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.