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Review and Therapeutic Approach to Malalignment of the Great Toenails: A Common Condition That Is Uncommonly Diagnosed.
Dermatol Surg
January 2025
Dermatology Professionals, Inc., East Greenwich, Rhode Island.
Article Synopsis
- Malalignment of the great toenails is a frequently overlooked nail disorder that is not often recognized in general medical practice.
- The study reviewed 34 articles involving 117 patients, all exhibiting lateral deviation of the toenails along with yellow-brown discoloration and thickening.
- The findings highlight the need for increased awareness among healthcare providers to improve diagnosis and management of this underdiagnosed condition.
Congenital syndactylies account for 1 to 2 out of 2000 birth defects. Although several types of syndactylies exist, we only studied embryonic syndactylies. The goal of our study was to compare 2 types of coverage flap for the reconstruction of the finger web spaces: a volar flap described by Blauth and a dorsal flap described by Gilbert.
View Article and Find Full Text PDFAcquired Asymptomatic Blue Tongue: A Report of Exogenous Agent-associated Tongue Dyschromia and Review of Blue Tongue Etiologies.
Cureus
November 2019
Dermatology, San Diego Family Dermatology, San Diego, USA.
This study presents the case of a man who developed a temporary and asymptomatic blue tongue. The dyschromia occurred following topical contact with gelato that contained Food, Drug, and Cosmetic (FD&C) blue dye no. 1.
View Article and Find Full Text PDF[Results of Blauth Palmar Flap in congenital syndactyly: Long-term outcome in a 31 webs study].
Ann Chir Plast Esthet
June 2020
SOS main Grenoble, unité de chirurgie réparatrice, de la main et des brûlés, hôpital A.-Michallon, CHU de Grenoble, avenue du Marquis-de-Grésivaudan, BP 217, 38043 Grenoble cedex 09, France. Electronic address:
Objectives: The main purpose of our study was to assess the web creep rate of congenital syndactyly treated with a Blauth palmar commissural flap.
Methods: Every child with at least one syndactyly, simple or complex, syndromic or not, were included in this study. The main criterion of this study was the web creep rate according to the Withey scale (0 to 4).
Unclassifiable pattern of hypopigmentation in a patient with mosaic partial 12p tetrasomy without Pallister-Killian syndrome.
Am J Med Genet A
July 2017
Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Article Synopsis
- - Pallister-Killian syndrome (PKS) is a genetic disorder caused by an extra chromosomal marker on chromosome 12, leading to various developmental issues and physical abnormalities.
- - A case study is presented of a 4-year-old girl with a significant presence of aneuploid cells, yet she exhibits only mild symptoms, showing a type of pigmentary mosaicism rather than the classic PKS phenotype.
- - This case suggests that even partial 12p chromosomal abnormalities can lead to milder manifestations than previously thought, indicating the need for better dermatologic evaluations to aid in genetic testing.
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