… Cardiac enzymes showed a lactate dehydrogenase (LDH) of 10480 u/l and a creatine
phosphokinase (CPK) of 288 u/l with normal creatine kinase isoenzyme containing M and B …

Objective Carbonic anhydrase (CA) II deficiency is a rare autosomal recessive disorder
caused by mutation in the CA II gene that leads to osteopetrosis, renal tubular acidosis (RTA), …

Results Fifty-six patients were initially diagnosed as having Sheehan’s syndrome for the 8-year
period studied. Six were eliminated because they did not fulfill the inclusion criteria. Of …

The case records of 50 patients with Sheehan’s syndrome were reviewed. All patients had
been treated at Riyadh Central Hospital. Analysis of the clinical and hormonal data revealed …

Actinomycosis bacteria are known for their disregard to anatomical boundaries and their
ability to infect organs all over the body including the liver. Here the infection is usually …

… Tarig S., Al Khuwaitir; Abdurahman M., Al Moghairi; Safia M., Sherbeeni; Abdullah S., Al
Ghamdi. …

Pycnodysostosis is a rare genetic disorder with a prevalence of 1.7 per million births; it usually
presents with short stature, osteosclerosis, increased bone fragility, and acro-osteolysis of …

Purpose To study the efficacy of lopinavir-ritonavir and hydroxychloroquine in critically ill
patients with coronavirus disease 2019 (COVID-19). Methods Critically ill adults with COVID-19 …

Four new zoonotic coronaviruses outbreak occurred in the past two decades. The first
coronavirus outbreak happened in 2003 and was named Severe Acute Respiratory Syndrome …