report of five cases of neuropleptic malignant syndrome

نویسندگان

اصغر الهی

asghar elahy , 1 jahan alley, taleghani ave. tehran, i. r. iran.تهران. خیابان طالقانی. نرسیده به خیابان دکتر شریعتی. کوچه جهان. پلاک 1. 2. روانپزشک. تهران. خیابان طالقانی. کوچه جهان. پلاک 1. پرویز مولوی

parviz moulavi , 1 jahan alley. taleghani ave. tehran, i. r. iran.تهران. خیابان طالقانی. کوچه جهان. پلاک 1.

چکیده

this paper reports five cases of neuroleptic malignant syndrome, admitted to shahid navab safavi psychiatric center during a period of six months. the onset and course of syndrome, types of drugs prescribed, and the variety of symptoms, were studied. results showed that early diagnosis of the syndrome, cessation of neuroleptic drugs, and classical treatment were efective in saving the lives of 3 out of 5 patients. there was also a correlation between dosage of the drugs and the incidence of the syndrome.

برای دانلود باید عضویت طلایی داشته باشید

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

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Lowe syndrome: report of five cases.

INTRODUCTION Lowe Syndrome, or Oculocerebrorenal Dystrophy (OCRL), has a recessive inheritance linked to X chromosome. It presents cataracts and glaucoma, delay in neuropsychomotor development, cognitive deficits, and renal Fanconi syndrome. OBJECTIVE Describe five patients with OCRL, attended at Tubulopathy outpatient clinic. METHOD We performed a retrospective assessment of 5 male patient...

متن کامل

Schwartz-Jampel syndrome: report of five cases.

We describe five patients with Schwartz-Jampel syndrome (SJS) examined at the outpatient service for neuromuscular disorders at our Institution from 1996 to 1999 with the objective of emphasizing the characteristic dysmorphic phenotype of SJS and its different clinical forms. Two cases presented SJS-type 1A, two had SJS-type 1B and one manifested SJS-type 2. Two boys with 3 and 13 years of age ...

متن کامل

Neuroleptic Malignant Syndrome : Report of 2 Cases

Neuroleptic malignant syndrome (NMS) is one of the rave but potentially fatal, idiosyncratic reaction to Neuroleptics and other medications (Smego and Durack, 1985). I t is characterised by fever, autonomic dysfunction, rigidity, altered conscious state with associated laboratory parameters like raised GPK, LDH, Hepatic enzymes, leucocytosis. This syndrome was first described by Delay and Denik...

متن کامل

Netherton syndrome: report of two cases

Netherton syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is trichorrhexis invaginata identified by microscopic examination of hair shaft. Ichthyosis linearis circumflexa is ano...

متن کامل

wolfram syndrome: report of five cases and review of literature

purpose: to report five cases of wolfram syndrome, an autosomal recessive neurodegenerative disease with ِdiabetes insipidus, diabetes mellitus, optic atrophy, and deafness (didmoad syndrome). patients and findings: all of the five patients had diabetes mellitus and optic atrophy. four patients had hearing loss. in spite of persistence of polyuria and polydipsia, diabetes insipidus had been prev...

متن کامل

brown-vialetto-van laere syndrome: report of five iranian cases

brown-vialetto-van laere syndrome (bvvls) is a rare neurological disorder of unknown etiology considered to be a form of motor neuron diseases. this syndrome is characterized by bilateral deafness and involvement of lower cranial nerves, especially 7th-12th. umn signs are less frequent. until 2007, only fifty eight cases were reported. half of the reported cases were sporadic. in the remaining ...

متن کامل

منابع من

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


عنوان ژورنال:
روانپزشکی و روانشناسی بالینی ایران

جلد ۲، شماره ۱، صفحات ۶۴-۷۱

کلمات کلیدی

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023