Cardiac Lesions in Children with "Hypercalcaemic" Facies
نویسنده
چکیده
The factors causing congenital heart disease, apart from the well known effects of rubella in the mother during the first three months of pregnancy, are in general obscure. The association of congenital heart disease with Multiple non-cardiac abnormalities may form the basis for an investigation }nto other aetiological factors. The combination of cardiac defects with mfantile hypercalcaemia is a fairly recent discovery; the exact nature of this association is still not understood. In 1956 Schlesinger, Butler, and Black drew attention to the occurrence of a characteristic facial appearance in mfants with severe hypercalcaemia, and in 1964 Beuren et al. drew attention to the syndrome of supra-aortic stenosis and a similar facial appearance. The connection between these two apparently unrelated syndromes was Pointed out by Black and Bonham Carter (1963), who found that patients Previously seen with infantile hypercalcaemia were presenting later in life with cardiac defects, particularly aortic stenosis. It has since been suggested that the cardiac defects may be the result of the deposition of calcium during the phase of hypercalcaemia.
منابع مشابه
بررسی توزیع هیپرائوزینوفیلی و بیماری عروق کرونر در مبتلایان به سندرم کاوازاکی در بخش کودکان بیمارستان امام خمینی (ره) تهران
Background: Kawasaki disease (KD) is an acute vasculitis in children. Eosinophilia, a reflection of the host's immune response that can cause tissue damage, has been associated with KD, with eosinophils preferentially accumulating in the microvasculature. In early-stage Kawasaki disease (KD), lesions (perivasculitis and vasculitis) first form in the microvessels, which can then extend to the la...
متن کاملسندرم نونان (گزارش یک مورد)
Noonan syndrome is a genetic condition inherited by an autosomally dominant manner, characterised by congenital heart disease, short stature, abnormal facies and the somatic feature of Turner's syndrome, but a normal karyotype. Noonan syndrome affects approximately 1 in 1500 live births. Congenital heart disease occurs in 35-50% of patients diagnosed with noonan syndrome. The most common cardia...
متن کاملDo you know this syndrome?*
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to Turner's syndrome phenotype. This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation. This article discusses the case of a 10 year-old patient with Noonan syndro...
متن کاملSurgical Treatment of Rheumatic Mitral Valve Lesions in Children and Adolescents
Rheumatismal lesions of the mitral valve a!I'e rare under the age of six and surgical irutervention in symptomatic patients is an academic problem. Early surgical treatment has been done to prevent serious changes and unreversib1e complications o.f the heart and lungs. From April 71 until April 74, thirty-five patient, ranging between 8-18 years of age, suffering of <lifferents heart ,tro...
متن کاملCardiac Biomarkers for Early Detection of Cardiac Involvement in Children with Kawasaki Disease: A Cross-Sectional Study
Background: Kawasaki disease (KD) is one of the most prevalent vasculitis diseases in children and can bring about serious cardiovascular complications. Early detection of cardiac involvement in KD can play an essential role in managing and preventing the cardiac sequels. We aimed to evaluate the applicability and diagnostic accuracy of cardiac biomarkers including car...
متن کامل