Austrian Syndrome: A Disease Of The Past?

Adams Oliver Syndrome and Congenital Deafness

Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic defor...

Austrian Syndrome: Triad of the Past or Harbinger of the Future?

گزارش 18 مورد بیمار مبتلا به سندرم شیهان

Sheehan’s syndrome has a broad spectrum of clinical and laboratory signs that range from nonspecific symptoms such as malaise, fatigue and anemia to severe hypophyseal insufficiency, which results in coma and death. We collected data from 18 patients diagnosed with Sheehan’s syndrome during the past 10 years. Patients profiles, including history, physical examination, clinical presentation that...

Pneumococcal pneumonia. Diagnostic, epidemiologic, therapeutic and prophylactic considerations.

T he past 50 years have witnessed striking changes in the physician’s perceptions of the clinical syndrome of pneumonia in general and of pneumococcal pneumonia in particular. Advances in basic and applied microbiology have contributed to increased awareness of the diversity of infectious agents which may invade the lung and ofthe complex interactions of viruses and bacteria in the pathogenesis...

A young girl with H syndrome and coeliac disease

H syndrome is an autosomal recessive genodermatosis with reports dating back to the last decade. This syndrome is caused by mutations in the SCL29A3 gene. The clinical characteristics of this syndrome consist of dermatological manifestations, including hyperpigmented, hypertrichotic, and indurated patches and plaques. It affects various systems by causing heart anomalies, hepatosplenomegaly, hy...