Propionic acidemia presenting as diabetic ketoacidosis.

نویسندگان

  • Rajesh Joshi
  • Ankur Phatarpekar
چکیده

adverse event reports by an expert advisory committee. Advisory Committee on Causality Assessment. Bull World Health Organ. 2000;78:178-85. 3. Dragos V, Mervic L, Zgavec B. Lichen striatus in a child after immunization. A case report. Acta Dermatovenerol Alp Panonica Adriat. 2006;15:178-80. 4. Moore K, Lam JM. The toddler with 1 striped leg: a linear papular rash. CMAJ. 2009; 28;180:947-8. 5. Vukiæeviæ J, Milobratoviæ D, Vesiæ S, MiloseviæJovæiæ N, Ciriæ D, Medenica L. Unilateral multiple lichen striatus treated with tacrolimus ointment: a case report. Acta Dermatovenerol Alp Panonica Adriat. 2009;18:35-8.

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

Isovaleric Acidemia Presenting as Diabetic Ketoacidosis: A Case Report

Isovaleric acidemia (IVA) is characterized by periodic vomiting, lethargy, coma, ketoacidosis and a 'sweaty feet' odor. Hyperglycemia, ketonemia, ketonuria and metabolic acidosis are the main clinical features of diabetic ketoacidosis (DKA) and these same symptoms can also be seen in acute attacks of metabolic diseases. We report a 2-year-old patient who presented with acute encephalopathy, hyp...

متن کامل

Neurologic nonmetabolic presentation of propionic acidemia.

BACKGROUND Patients with propionic acidemia usually present in the neonatal period with life-threatening ketoacidosis, often complicated by hyperammonemia. It was thought that the neurologic abnormalities seen in this disease were exclusively the consequences of these acute crises. Experience with 2 patients with propionic acidemia indicates that this disease may present first with prominent ne...

متن کامل

Cerebral CT Findings in Methylmalonic and Propionic Acidemias 955

The cerebral computed tomographic findings in two infants with methylmalonic acidemia and one infant and one adult with propionic acidemia are presented. Pertinent metabolic, clinical, and pathologic features of these genetic disorders of vitamin B'2 (cobalamin) and biotin metabolism are reviewed briefly. Computed tomographic abnormalities consist of focal or diffuse deep cerebral hemisphere lu...

متن کامل

"Tandem ICON hCG" urine pregnancy test evaluated.

492 CLINICAL CHEMISTRY, Vol.31, No. 3, 1985 1. Fishlock RC, Bieber LL, Snoswell AM. Sources of error in determinations of carnitine and acylcarnitine in plasma. Clin Chem 30, 316-318 (1984). 2. Brass EP, Hoppel CL. Carnitine metabolism in the fasting rat. J Biol Chem 253, 2688-2693 (1978). 3. Genuth SM, Hoppel CL. Plasma and urine carnitine in diabetic ketosis. Diabetes 28, 1083-1087 (1978). 4....

متن کامل

Biotin responsive multiple carboxylase deficiency presenting as diabetic ketoacidosis.

Multiple carboxylase deficiency (MCD) is a rare inherited metabolic disease of biotin dependency due to deficiency of holocarboxylase synthetase (HCS) or biotinidase deficiency. A 30-month-old female patient who presented with the initial features of diabetic ketoacidosis (severe metabolic acidosis, ketosis, and hyperglycemia), lactic acidemia, moderate hyperammonemia, and generalized organic a...

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 48 2  شماره 

صفحات  -

تاریخ انتشار 2011