Results 31 to 40 of about 919,358 (274)
Congenital pyloric atresia and epidermolysis bullosa: Report of a rare association
Pyloric atresia (PA) is an unusual congenital disorder that accounts for about 1% of all intestinal atresia, with an incidence around 1 in 100,000 live births. PA may occur as an isolated disorder or may be associated with epidermolysis bullosa (EB).
Pradyumna Pan
doaj +1 more source
Skin fragility and abnormal liver function tests [PDF]
A 53-year-old man, a worker in a plastic factory, presented with a 12-month history of a non-itchy skin rash on the dorsum of both hands, associated with increased skin fragility and tendency to recurrent scar formation. The biochemical profile revealed an isolated elevation of serum alanine aminotransferase 55 IU/l (normal 5–36 IU/l).
S, Chitturi, M, Dakkak, A P, Campbell
openaire +2 more sources
Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome and ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) syndrome are two rare autosomal dominant disorders caused by heterozygous mutations occurring in the TP63 gene.
NC DOCKS at East Carolina University +1 more
core
Fragility, conflict, and migration
Fragility, Conflict, and Migration addresses challenges to livelihood, food, and climate security faced by some of the most vulnerable populations worldwide.
Kosec, Katrina; Laderach, Peter; and Ruckstuhl, Sandra +1 more
core
Ehlers-Danlos Syndrome Type VIIC: A Mexican Case Report
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders whose primary clinical features include soft and extensible skin, articular hypermobility and tissue fragility.
Ana Rosa Rincón-Sánchez +12 more
doaj +1 more source
Skin-to-skin parental contact with fragile preterm infants
Abstract Skin-to-skin contact has been implemented recently to facilitate maternal-infant bonding of preterm infants. The technique allows the removal of fragile preterm infants from an incubator to the bare chest of a parent or caretaker.
G M, Cleary +3 more
openaire +2 more sources
Skin fragility and blistering due to use of sunbeds [PDF]
6 observations de fragilisation de la peau et de formation de phlyctenes apres irradiation par ultraviolets pour ...
P M, Farr +3 more
openaire +2 more sources
Background: Epidermolysis bullosa (EB) with congenital absence of skin (CAS) (Bart syndrome) is a rare condition characterized by the coexistence of any form of EB and congenital localized absence of skin, also known as aplasia cutis congenita
Danya Alwafi +3 more
doaj +1 more source
The diagnosis and management of porphyria cutanea tarda (PCT)
The porphyrias are a group of disorders in which excessive quantities of porphyrins or their precursors are produced. They are due to abnormalities in the control of the porphyrin-haem metabolic pathway.
Mojakgomo H. Motswaledi
doaj +1 more source
Inherited epidermolysis bullosa is a heterogeneous group of hereditary skin diseases characterized by skin (mucosa) fragility, which leads to blistering.
Li Zhang +3 more
doaj +1 more source

