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1.
Bahrain Medical Bulletin. 2018; 40 (2): 129-131
Dans Anglais | IMEMR | ID: emr-197027

Résumé

Prader-Willi syndrome [PWS] typically presents during the neonatal period as hypotonia with poor feeding and is confused with neonatal sepsis; however, these patients eventually develop special facial characteristics and gain weight dramatically. Some of these patients can have autistic behaviors that manifest as loss of social interest, poor communication as well as repetitive movements. We present a case of a five-year-old female who developed hypotonia and poor reflexes soon after birth and was noticed to have Intrauterine Growth Restriction [IUGR]. Two months later, she was noticed to have dysmorphic features with delayed developmental milestones. At 30 months, she was diagnosed with obesity and obstructive sleep apnea. At three years, she was diagnosed which raised the suspicion of autism.with PWS and at five years of age, she developed autistic behaviors

2.
Bahrain Medical Bulletin. 2017; 39 (3): 187-188
Dans Anglais | IMEMR | ID: emr-188433

Résumé

Pulmonary tuberculosis could be associated with certain types of anemia, such as normocytic normochromic anemia and microcytic hypochromic anemia; however, it is rarely associated with autoimmune hemolytic anemia


We report a case of a child with pulmonary tuberculosis associated with autoimmune hemolytic anemia and iron deficiency anemia which was resolved with anti-tuberculosis medications, isoniazid, pyrazinamide, rifampicin and ethambutol


Sujets)
Humains , Femelle , Enfant , Anémie hémolytique auto-immune/étiologie , Anémie hypochrome , Anémie par carence en fer , Antituberculeux
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