Results 51 to 60 of about 1,348 (172)
Respirology Case Reports, Volume 13, Issue 11, November 2025.Laryngo‐onycho‐cutaneous syndrome (LOCS), or Shabbir's syndrome, linked to mutations in the LAMA3 gene, is predominantly observed in children from Punjabi families. We present the case of a 2.5‐year‐old male with LOCS who was initially misdiagnosed with asthma due to progressive hoarseness and stridor.
Nabeel Ahmad +8 more
wiley +1 more source
Photo gallery of onychodystrophies
Russian Journal of Skin and Venereal Diseases, 2020 Onychodystrophies are various pathological processes in the nail apparatus of infectious and non-infectious nature, related to changes in its morphology. The most common cause of nail changes is a fungal infection. However, onychodystrophy can be a manifestation of dermatological diseases, trauma, medication, systemic and tumor processes.
openaire +1 more source
Glucagonoma and Glucagonoma Syndrome: An Updated Review
Clinical Endocrinology, Volume 103, Issue 4, Page 417-426, October 2025.ABSTRACT Background Glucagonoma is a rare well‐differentiated slowly proliferating pancreatic neuroendocrine tumour, characterized by several manifestations including necrolytic migratory erythema, weight loss, diabetes and anaemia. Aim The purpose of the current review was to acknowledge literature about this rare tumour discerning the clinical ...
Sofia Anelli +8 more
wiley +1 more source
The Network of Mystery: Unraveling Atypical Dermatopathia Pigmentosa Reticularis
Clinical Dermatology ReviewDermatopathia pigmentosa reticularis (DPR) is a rare ectodermal dysplasia characterized by generalized reticulate hyperpigmentation, nonscarring alopecia, and onychodystrophy, caused by autosomal dominant mutations in KRT14. Fewer than 25 cases have been
Spandana Devarahalli Krishnamurthy +3 more
doaj +1 more source
EBioMedicine, 2019 Background: Dominant deafness-onychodystrophy (DDOD) syndrome is a rare disorder mainly characterized by severe deafness, onychodystrophy and brachydactyly.
Weihao Zhao +9 more
doaj +1 more source
Steroid responsive mononeuritis multiplex in the Cronkhite-Canada syndrome
Frontiers in Neurology, 2016 The Cronkhite-Canada syndrome (CCS) is a rare disorder of unknown origin characterized by generalized gastrointestinal polyposis, alopecia, hyperpigmentation and onychodystrophy.
YL Lo, KH Lim, XM Cheng, S Mesenas
doaj +1 more source
Microscopic examination of normal nail clippings
Dermatology Practical & Conceptual, 2013 Background: Nail clipping analysis for diagnosing causes of onychodystrophy other than onychomycosis is investigated to a very small extent. In order to achieve acceptance as a diagnostic method for any kind of nail abnormalities, normal microscopic ...
Betina Werner, Andre Antunes
doaj +1 more source
Dermatopathia pigmentosa reticularis: Report of a new cases and literature review
Indian Journal of Dermatology, 2016 Dermatopathia pigmentosa reticularis (DPR) is a very rare autosomal dominant ectodermal dysplasia caused by mutations in keratin 14 and characterized by the triad of generalized reticulate hyperpigmentation, nonscarring alopecia, and onychodystrophy.
Fahad Al Saif
doaj +1 more source
Dermatopathia pigmentosa reticularis
Indian Journal of Paediatric Dermatology, 2018 Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Gauri Vats +3 more
doaj +1 more source
Successful treatment of median canaliform nail dystrophy with topical tazarotene foam
JAAD Case Reports, 2022 Eugenie Y. Quan, MD +1 more
doaj +1 more source