منابع مشابه
Cyanosis in Congenital Heart Disease
Background: CKMB, the cardiac-specific heterodimer of cytosolic creatine-kinase (CK), is developmentally and physiologically regulated, tissue hypoxia being a proposed regulator. In patients with cyanotic heart disease the myocardium is perfused with partially saturated blood. We questioned whether the myocardium of cyanotic subjects contains higher proportions of CKMB. Materials and Methods: C...
متن کاملA Case of Enterogenous Cyanosis
flatulence with marked borborygmi, abdominal pain and diarrhoea began, and have continued ever since. His motions watery and undigested, three to seven a day> were associated with griping pains before and after. yn exertion he had difficulty in breathing and pain over the praecordia, his legs became stiff and he had to stop and rest. He complained also of more or less constant peculiar pulling ...
متن کاملA case of unexplained cyanosis.
It is now clear that hepatopulmonary syndrome (HPS) may occur and contribute significantly to gas exchange abnormalities in the setting of other cardiopulmonary abnormalities. Since there is no gold-standard diagnostic test for HPS, diagnosis rests on documenting arterial oxygenation abnormalities resulting from intrapulmonary vasodilatation in the setting of liver disease. Retrospective studie...
متن کاملCongenital methemoglobinemia: a rare cause of cyanosis in the newborn--a case report.
Cyanosis is a physical finding that can occur at any age but presents the greatest challenge when it occurs in the newborn. The cause is multiple, and it usually represents an ominous sign, especially when it occurs in association with neonatal sepsis, cyanotic congenital heart disease, and airway abnormalities. Cyanosis caused by abnormal forms of hemoglobin can also be life-threatening, and e...
متن کاملWhy so blue? A case of neonatal cyanosis due to congenital methaemoglobinaemia (HbM Iwate).
To cite: McGrath JS, Datir S, O’Brien F. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016216805 DESCRIPTION A 2.18 kg male baby was born by elective caesarean section at 34+3 weeks to a primiparous mother with autosomal dominant congenital methaemoglobinaemia (HbM Iwate) and gestational diabetes. Having been asymptomatic throughout her life, she developed sign...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1926
ISSN: 0035-9157
DOI: 10.1177/003591572601900204