Results 41 to 50 of about 57,398 (258)
Background/Objectives: Lymphedema, a common source of disability among oncology patients, necessitates continuous targeted rehabilitation. Recent studies have revealed the role of connective tissue in this pathology; however, despite existing research on
Carmelo Pirri +6 more
doaj +1 more source
Idiopathic Calcinosis Cutis over Elbow in a 12-Year Old Child
Calcinosis cutis is an uncommon disorder caused by an abnormal deposit of calcium phosphate in the skin in various parts of the body. Four main types of calcinosis cutis have been recognized according to etiology: associated with localized or widespread ...
S. K. Venkatesh Gupta +2 more
doaj +1 more source
Aplasia Cutis Congenita as a Sole Manifestation of Congenital Varicella Syndrome
Aplasia cutis congenita following maternal varicella is well known. On the other hand, aplasia cutis congenita as the sole manifestation of congenital varicella syndrome is very rare. A perusal of the literature revealed only one case.
Alexander K. C. Leung +2 more
doaj +1 more source
A developmental and genetic classification for malformations of cortical development: update 2012. [PDF]
Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopmental delay and epilepsy. In addition, study of these disorders contributes greatly to the understanding of normal brain
Barkovich, A James +4 more
core +3 more sources
This study retrospectively analysed eight years of neonatal spinal ultrasound data from a major Australian children's hospital to assess the value of imaging for simple sacral dimples. Out of 448 scans, 195 were for an isolated simple dimple, and only two infants (1%) were found to have spinal dysraphism, both with other congenital anomalies.
Nyles Tattersall +5 more
wiley +1 more source
The Primacy of Ethics in Aesthetic Medicine: A Review
Background:. The landscape of modern aesthetic medicine has witnessed a paradigm shift from traditional doctor-led care to a consumer-driven model, presenting a plethora of ethical challenges.
Sylvia Ramirez, MD, MPH, MBA +3 more
doaj +1 more source
Keratoglobus with ARCL1B (EFEMP2 gene) cutis laxa
Purpose: To report a case of keratoglobus in a patient with autosomal recessive (AR) cutis laxa. Observations: A 38 year old male presented with decreased vision in both eyes uncorrectable with spectacles and a history of corneal rupture in the left eye ...
Thomas F. Mauger +3 more
doaj +1 more source
Introdução:A cutis laxa é uma doença rara do tecido conjuntivo provocada por alterações da elastina. Caracteriza-se por pele sem elasticidade, flácida, mole e enrugada, dando aos doentes um aspecto envelhecido; o envolvimento sistémico é variável ...
Afonso, A +5 more
core
Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 region [PDF]
Mutations in ABCC6 cause pseudoxanthoma elasticum (PXE), a heritable disease that affects elastic fibers. Thus far, >200 mutations have been characterized by various PCR-based techniques (primarily direct sequencing), identifying up to 90% of PXE-causing
Chassaing, N +9 more
core +2 more sources
Concurrent Psoriasis and Dermatomyositis: Retrospective Analysis and Literature Review
ABSTRACT Background Psoriasis (PsO) and dermatomyositis (DM) are both autoimmune‐mediated, inflammatory conditions. The concurrence of PsO and DM is rare, and literature on their relationship remains limited. Additionally, cutaneous DM can be challenging to clinically diagnosis, often presenting with psoriasiform clinical features.
Emily R. Gordon +5 more
wiley +1 more source

