Results 21 to 30 of about 8,005 (109)
Conservative Restoration of Bone Without Casting or Surgery for Charcot Foot in a Diabetic Patient
This case highlights the successful management of a 52‐year‐old male with poorly controlled diabetes and Charcot neuroarthropathy. Early diagnosis and a holistic treatment plan, including antibiotics, vitamins, and local interventions, improved the ...
Mutasem Iqnaibi +5 more
doaj +1 more source
Autoimmune progesterone dermatitis is considered a rare cyclical autoimmune reaction to endogenous progesterone in fertile females that is characterized by skin lesions ranging from mild urticaria to anaphylaxis.
Ibrahim Alheeh +4 more
doaj +1 more source
Congenital hiatal hernia is a rare congenital defect and often occurs at a sporadic basis, but familial cases have also been reported. Here, we report on a 3-year-old male patient of Middle-Eastern descent, diagnosed at 5 months of age patient presenting
Ramzi H Mujahed +6 more
doaj +1 more source
This study examines the relationship between rotating shift work and burnout among nurses in Hebron hospitals within the context of Palestine's unique political and social conditions.
Yousef Jaradat +7 more
doaj +1 more source
Posterior Epistaxis Presenting as Upper GI Bleeding in A Healthy 21‐Year‐Old Patient: A Case Report
A 21‐year‐old Palestinian woman experienced recurrent hematemesis and melena over 7 months, requiring multiple hospital admissions and blood transfusions. Despite extensive investigations, the bleeding source remained undetermined until a posterior nasal
Aref AlRajabi +5 more
doaj +1 more source
Extremely Rare Neonatal Case With Pyloric Atresia, Heart Defects, Hypotonia, Jaundice, and Acidosis
Pyloric atresia (PA) is an exceptionally rare congenital cause of gastric outlet obstruction, often associated with syndromic conditions such as epidermolysis bullosa (EB).
Saja Abouodeh +7 more
doaj +1 more source
A 30‐year‐old woman with recurrent pancreatitis and nephrolithiasis was diagnosed with chronic calcific pancreatitis linked to primary hyperparathyroidism (PHPT).
Kareem Ibraheem +5 more
doaj +1 more source
Congenital dyserythropoietic anemia type III (CDA III) is an extremely rare inherited disorder characterized by ineffective erythropoiesis, multinucleated erythroblasts in the bone marrow, and variable clinical gravity. We report the case of a 6‐year‐old
Ahmad Hamammdi +5 more
doaj +1 more source
Transrectal Endoscopic Ultrasound‐Guided Pelvic Abscess Drainage (EUS‐PAD) is a minimally invasive technique for treating pelvic abscesses, especially those that are difficult to reach.
Kareem Ibraheem +6 more
doaj +1 more source
Testicular tumors are rare in children, accounting for only 1% to 2% of pediatric solid tumors. Mature teratomas (MTs) are a benign subtype that typically occur in prepubertal boys and may occasionally mimic hydroceles.
Rahaf W. Thabaineh MD +6 more
doaj +1 more source

