Results 91 to 100 of about 19,416 (274)
Eosinofiilne gastroenteriit seedetrakti vaevuste ühe põhjusena [PDF]
Eosinofiilne gastroenteriit on harva esinev, täpselt teadmata põhjuse ja tekkemehhanismiga, ägenemiste ning remissioonidega kulgev krooniline haigus. Sellele haigusele on iseloomulik seedetrakti erinevate vaevuste ja sümptomite esinemine,
Ress, Krista, Uibo, Oivi
core +2 more sources
ABSTRACT Background Filamin A (FLNA) deficiency is a known cause of progressive lung disease and need for pediatric lung transplant; however, what may be less well known to lung transplant providers are the extrapulmonary complications of FLNA deficiencies, such as wandering spleen.
Savannah Ellis Knight+2 more
wiley +1 more source
Exclusive pyloric stenosis: A rare presentation of gallbladder cancer
We report a case of gallbladder cancer, which presented exclusively as tight pyloric stenosis. The patient had persistent vomiting, severe weight loss, and esophageal symptoms due to gastric reflux.
Suhas Durganand Wagle+2 more
doaj +1 more source
Life-threatening electrolyte abnormalities in pyloric stenosis
Infantile hypertrophic pyloric stenosis (IHPS) is an idiopathic disorder of infancy where the hypertrophic and enlarged pyloric muscle causes gastric obstructive symptoms of progressive emesis leading to hypochloremic, hypokalemic, metabolic alkalosis ...
Christopher Jacobs+3 more
doaj +1 more source
William Edwards Ladd, M.D. (1880-1967): the description of his bands. [PDF]
In the early 20th century, an established surgical specialty catering to pediatric surgery did not exist, and pediatric surgical ailments were operated on by general surgeons.
Cowan, MD, Scott W.+4 more
core +1 more source
A case report of cornelia de lange syndrome in Northern Iran; a clinical and diagnostic study [PDF]
As a rare multisystem congenital anomaly disorder, Cornelia de Lange syndrome (CdLS) is featured by delayed growth and development, distinct facial dimorphism, limb malformations and multiple organ defects.
Alaee, E.+2 more
core +1 more source
Extremely Rare Neonatal Case With Pyloric Atresia, Heart Defects, Hypotonia, Jaundice, and Acidosis
ABSTRACT Pyloric atresia (PA) is an exceptionally rare congenital cause of gastric outlet obstruction, often associated with syndromic conditions such as epidermolysis bullosa (EB). This case highlights a diagnostically challenging presentation of *non‐syndromic pyloric atresia* in a neonate, complicated by a moderate mid‐muscular ventricular septal ...
Saja Abouodeh+7 more
wiley +1 more source
Postoperative pain management in children: Guidance from the pain committee of the European Society for Paediatric Anaesthesiology (ESPA Pain Management Ladder Initiative) [PDF]
The main remit of the European Society for Paediatric Anaesthesiology (ESPA) Pain Committee is to improve the quality of pain management in children. The ESPA Pain Management Ladder is a clinical practice advisory based upon expert consensus to help to ...
Adamek+196 more
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Adult idiopathic hypertrophic pyloric stenosis
Idiopathic hypertrophic pyloric stenosis (IHPS) is a predominantly infantile disease. The adult type of IHPS is extremely rare but it has been well recognized since the 19th century.
Hsien-Ping Lin+2 more
doaj +1 more source