• Nenhum resultado encontrado

[PDF] Top 20 A case report of Cotard’s syndrome with catatoniform symptoms

Has 10000 "A case report of Cotard’s syndrome with catatoniform symptoms" found on our website. Below are the top 20 most common "A case report of Cotard’s syndrome with catatoniform symptoms".

A case report of Cotard’s syndrome with catatoniform symptoms

A case report of Cotard’s syndrome with catatoniform symptoms

... depressive symptoms had began 18 months before: she presented sadness, anhedonia and easy crying, which got progressively worse, with apathy, restlessness, prejudice in her daily activities, insomnia, ... See full document

2

Goldbloom's Syndrome - a case report

Goldbloom's Syndrome - a case report

... hospital with one month history of pain localized to the limbs’ diaphysis, refusal to walk, inter- mittent fever and weight loss (two ...peak of fever (maximum 38 °C), anorexia, fatigue, cutaneous ... See full document

5

Generalized Lichen nitidus associated with Down's syndrome: case report

Generalized Lichen nitidus associated with Down's syndrome: case report

... disease of unknown etiology, characterized by flesh-colored, shiny papules of 1-2 mm and generally asymptomatic or with mild ...sites of occurrence are genitalia, upper limbs, trunk and ... See full document

3

MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME ASSOCIATED WITH PRUNE BELLY SYNDROME: A CASE REPORT

MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME ASSOCIATED WITH PRUNE BELLY SYNDROME: A CASE REPORT

... visualization of both the ...duodenum with duodenojejunal junction to the right of vertebra and caecum in the left hypochondrium confirming ...microcolon with small bowel dilatation upto ... See full document

3

ALPORT’S SYNDROME: A CASE REPORT

ALPORT’S SYNDROME: A CASE REPORT

... Alport's syndrome is considered to be a widespread disorder of basement membrane, clinically characterised by haematuric nephritis, sensorineural deafness and ocular ...we report a case ... See full document

3

Polyglandular Autoimmune Syndrome Type III with Primary Hypoparathyroidism

Polyglandular Autoimmune Syndrome Type III with Primary Hypoparathyroidism

... autoimmune syndrome is defined as multiple endocrine gland insufficiencies accompanied by autoimmune diseas- es of the endocrine and nonendocrine ...a case of nontuberculosis adrenal gland ... See full document

5

The coexistence of focal segmental glomerulosclerosis with carcinoid syndrome: A case report

The coexistence of focal segmental glomerulosclerosis with carcinoid syndrome: A case report

... 2. Calvo Villas JM, Morales Umpierrez A, Ramirez Sanchez MJ, et al.. Focal and segmental glomerulosclerosis and non-Hodgkin’s lymphoma. Clin Nephrol 2002;57:173-174. 3. Lin FC, Chen JY, Yang AH. The association of ... See full document

2

CASE REPORT HEMOPHAGOCYTIC SYNDROME ASSOCIATED WITH HEPATITIS A: CASE REPORT AND LITERATURE REVIEW

CASE REPORT HEMOPHAGOCYTIC SYNDROME ASSOCIATED WITH HEPATITIS A: CASE REPORT AND LITERATURE REVIEW

... prognosis of the VAHS is mainly based in the severity and duration of the ...risk of severe infections, including gram-positive bacteria, such as ...because of the possibility of ... See full document

5

Thoracic outlet syndrome (TOS) mimicking Takayasu´s arteritis - case report

Thoracic outlet syndrome (TOS) mimicking Takayasu´s arteritis - case report

... associated with a painful lesion on the second digital pulp in the last two ...associated with new necrotic lesion on the third finger of the left ...treated with cilostazol, ace- tylsalicylic ... See full document

6

A Case Report of Mauriac Syndrome: Diabetic Dwarfs.

A Case Report of Mauriac Syndrome: Diabetic Dwarfs.

... (252.6) with normal FT3, ...iron, S. ferritin were normal. Ultrasound abdomen showed fatty liver with atrophic pancreas and USG neck showed bilateral bulky thyroid ... See full document

3

Rev. Assoc. Med. Bras.  vol.62 número3

Rev. Assoc. Med. Bras. vol.62 número3

... we report a case of DRESS syndrome in a 20-year old female pa- tient, black, former alcoholic and former user of cocaine, with epilepsy and non-speciied neuropsychiatric disor- ... See full document

4

case report: Werner’s Syndrome

case report: Werner’s Syndrome

... Werner’s syndrome (WS) is an extremely rare and au- tosomal recessive premature aging syndrome charac- terized by scleroderma-like skin changes, alopecia, leg ulcers, short stature, cataract, early ... See full document

5

Sneddon's syndrome: case report and review of its relationship with antiphospholipid syndrome

Sneddon's syndrome: case report and review of its relationship with antiphospholipid syndrome

... Sneddon’s syndrome is a rare disorder characterized by the occurrence of cerebrovascular disease associated with livedo ...antiphospholipid syndrome is the most frequent type of ... See full document

3

Rev. Bras. Anestesiol.  vol.65 número4

Rev. Bras. Anestesiol. vol.65 número4

... Case report: We report the case of a 24-h-old newborn with Goldenhar’s ...atresia with distal tracheoesophageal ...intubation with fibrobronchoscope distal to the ... See full document

4

Waardenburg Syndrome: A Report of Two Familial Case Series

Waardenburg Syndrome: A Report of Two Familial Case Series

... management of this syndrome has been solely focused on addressing sensorineural hearing loss by cochlear implants if detected at an early age, the occurence of reduced vision, problems related to the ... See full document

4

Rev. Bras. Anestesiol.  vol.65 número5

Rev. Bras. Anestesiol. vol.65 número5

... Jarcho Levine syndrome is a rare congenital disorder cha- racterized by distinctive vertebral anomalies. Vertebral anomalies and defects in the costovertebral fusion result in a smaller thoracic cavity and ... See full document

3

Braz. j. .  vol.79 número2 en v79n2a20

Braz. j. . vol.79 número2 en v79n2a20

... Tolosa-Hunt syndrome was first des- cribed in 1954, in the case report of a patient with painful ophthalmoplegia caused by nonspecific granulomatous inflammation of the cavernous ... See full document

1

Cantrell Syndrome. Case report of an adult

Cantrell Syndrome. Case report of an adult

... condition, with jugular stasis ++ at 45º, hemangioma at the left hemifa- cies, a xiphoid appendix noticeable on palpation, a flaw in the coaptation of the left lower costal arches, and with evi- dent ... See full document

3

Plummer-Vinson syndrome: a case report.

Plummer-Vinson syndrome: a case report.

... A síndrome de Plummer-Vinson (SPV), também conhecida como síndrome de Paterson-Kelly ou disfagia sideropênica, é conhecida pela presença da tríade clássica de disfagia cervical, anemia f[r] ... See full document

2

Peutz-Jeghers syndrome: case report.

Peutz-Jeghers syndrome: case report.

... Peutz-Jeghers syndrome (PJS) is a dominant autosomal inherited disorder characterized by intestinal hamartomatous polyps in association with mucocutaneous melanocytic ...This syndrome is rare, and ... See full document

2

Show all 10000 documents...