Treatable cause of ventricular dysfunction in DiGeorge syndrome.

نویسندگان

  • Neeraj Awasthy
  • Sanjay Khatri
چکیده

Hypocalcemia is a known cause of reversible cardiomyopathy and DiGeorge syndrome is an important cause of hypocalcemia. A 17 days old 2.3 kg female child, first in birth order, born to a primigravida mother by full term LSCS started having tonic-clonic jerks on day 8 of life and was also noticed to have bluishness of lips and nails, when she was referred to us. Child had intermittent episodes of tonic clonic seizures on admission. On examination, her hemodynamic parameters were stable; saturation was 74% in room air and there was cyanosis. Precordial examination revealed no cardiomegaly. S1was normal, S2 was single. There was a continuous murmur at infraclavicular area. Per abdomen – liver 2cm below right costal margin. Rest of the systemic examination was unremarkable. Echocardiography revealed pulmonary atresia with ventricular septal defect (VSD) with biventricular dysfunction (LVEF = 35%). Blood investigations revealed hypocalcemia (calcium = 4 mg/dL) for which correction was given intravenously. Qtc of the patient was 540 milliseconds. She underwent CT pulmonary angiography which revealed atresia of main pulmonary artery and hypoplastic confluent pulmonary arteries, VSD, two moderate size aorto-pulmonary collateral and aberrant right subclavian artery; thymus was not seen. FISH test showed Di-George Syndrome. Mother sample for calcium and alkaline phosphatase was within normal limits (calcium=9.5mg/dL, alkaline phosphatase = 144u/L). At discharge on oral calcium, there was marked improvement in ventricular function (LVEF = 50%) with no recurrence of seizure activity. As the baby was maintaining a saturation of about 86% it was advised to follow up for saturation monitoring and surgery at a later date. 22q11.2 deletion syndrome has several presentations including DiGeorge syndrome (DGS). Hypocalcemia is relatively common in children with DiGeorge syndrome with incidence rates varying from 17 to 60%. Especially young infants have a high incidence of hypocalcemia. Myocardial dysfunction in patients with hypocalcemia is well described in the literature [1-4] but their association has been reported scantily [1,2].

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.

DiGeorge syndrome was diagnosed in an infant who had an interrupted aortic arch, hypoparathyroidism, and low T lymphocyte numbers. Two siblings had heart defects that are not commonly described in DiGeorge syndrome (a membranous ventricular septal defect and coarctation of the aorta respectively). These siblings did not have evidence of thymic dysfunction or hypoparathyroidism. Chromosome analy...

متن کامل

Digeorge syndrome presenting with uncommon cardiac anomaly and hepatomegaly

Digeorge syndrome is caused by microdeletion of a large region of chromosome 22q11.2 lead to the abnormal development of the third and fourth pharyngeal pouches. This syndrome is characterized by hypoparathyroidism, cellular immune deficiency secondary to thymic hypoplasia, congenital heart disease and dysmorphic facial features. In this case report, we describe a 4month old boy who presented w...

متن کامل

گزارش موردی سندرم شیهان همراه با پان سیتوپنی

Background & Aims: Sheehan’s syndrome is defined as anterior pituitary dysfunction due to postpartum ischemic necrosis of the pituitary gland after massive bleeding. Hematologic abnormalities such as normochromic anemia have been reported in these patients. However, pancytopenia is rarely observed. Case presentation: We describe the case of a 30-year-old woman with generalized weakness, ...

متن کامل

Correlation between the Level of Creatinine, Serum Cardiac Troponines and Left Ventricle Function Tests in Patients with Chronic Renal Diseases without Acute Coronary Syndrome

Background and Objectives:  The aim of this study was to survey the relationship between the level of  creatinine,cardiac troponins serum and the function of  the left ventricle in patients with  kidney insufficiency,without acute coronary syndrome. Materialsand Methods:The sample  was150 patients with nondialysis chronic kidney disease without  acute  coronary  syndrome,  hospitalized  at  I...

متن کامل

Tachycardiomyopathy: a diagnosis not to be missed.

The prognosis of dilated cardiomyopathy is generally poor. In the vast majority of cases the cause of the ventricular dysfunction is irreversible but occasionally potentially curable causes are identified. Tachycardiomyopathy is a rare and potentially treatable cause of heart failure. A patient with a particularly severe case who had an excellent outcome is presented.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Indian pediatrics

دوره 50 9  شماره 

صفحات  -

تاریخ انتشار 2013