• No results found

[PDF] Top 20 How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report

Has 10000 "How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report" found on our website. Below are the top 20 most common "How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report".

How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report

How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report

... with schizophrenia according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV, previously used the Third ... See full document

5

Seizures as the first manifestation of chromosome 22q11 2 deletion syndrome in a 40 year old man: a case report

Seizures as the first manifestation of chromosome 22q11 2 deletion syndrome in a 40 year old man: a case report

... The 12-lead electrocardiogram showed a prolonged cor- rected QT interval. Echocardiogram, abdominal ultra- sound and electroencephalogram were normal. A computer tomography of the brain showed basal ganglia calcification ... See full document

5

Anatomic Malformations of the Middle and Inner Ear in 22q11 2 Deletion Syndrome: Case Series and Literature Review

Anatomic Malformations of the Middle and Inner Ear in 22q11 2 Deletion Syndrome: Case Series and Literature Review

... 300 patients followed at the University Medical Center Utrecht and the 1300 patients from Children’s Hospital of Philadelphia, 26 patients (52 ears), 14 males and 12 females, un- derwent radiologic ... See full document

7

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

... in patients with schizophrenia with a commensurate increase in negative symptoms during withdrawal from antipsychotic medications (Walker et ...of patients with schizophrenia (Saetre et ...in ... See full document

8

Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era

Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era

... Abstract: Schizophrenia is a complex neuropsychiatric disease with documented clinical and genetic heterogeneity, and evidence for neurodevelopmental ...with schizophrenia, in targeted studies over two ... See full document

18

Two patients with chromosome 22q11 2 deletion presenting with childhood obesity and hyperphagia

Two patients with chromosome 22q11 2 deletion presenting with childhood obesity and hyperphagia

... 22q11.2 deletion syndrome is a clinically heterogeneous condition of intellectual disability, parathyroid and thyroid hypoplasia, palatal abnormalities, cardiac malformations and psychiatric ...Prader-Willi ... See full document

7

22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

... 22q11.2 deletion syndrome (22q11DS) is caused by an autosomal dominant microdeletion of chromosome 22 at the long arm (q) ...the deletion, and is associated with an increased risk of psychiatric ... See full document

12

Marfan syndrome with acute abdomen: a case report

Marfan syndrome with acute abdomen: a case report

... Although MFS is a multisystem disorder, the most clinically significant manifes- tation is cardiovascular disease. Because of the abnormal supporting tissues of the aorta and cardiac valves, individuals with MFS are ... See full document

5

Neural correlates of reward processing in adults with 22q11 deletion syndrome

Neural correlates of reward processing in adults with 22q11 deletion syndrome

... A deletion at ...with 22q11 deletion syndrome (22q11DS) carry a 25- to 30-fold increased risk of psychosis ...benefit patients with 22q11DS but also could help patients with ... See full document

12

Dentigerous Cyst with Odontome: A Case Report

Dentigerous Cyst with Odontome: A Case Report

... The prognoses of most dentigerous cysts are excellent with lesser percentage of recurrence. Hence prompt diagnosis and management can prevent various complications, because if left untreated dentigerous cysts interrupt ... See full document

5

22q11 deletion syndrome : parents' and children's experiences of educational and healthcare provision in the UK

22q11 deletion syndrome : parents' and children's experiences of educational and healthcare provision in the UK

... Despite many receiving educational support, 91% of our respondents reported difficulties with learning at school. These include both curricular difficulties and general difficulties as shown in Figure 2. ... See full document

17

The antiphospholipid antibody syndrome: a case report

The antiphospholipid antibody syndrome: a case report

... The patient reappeared 2 months later with persistent abdominal pains, this time associated with distention of 2 weeks’ duration. On examination, the patient had lost a considerable amount of weight and had ... See full document

5

Hyposmia, symptoms of REM sleep behavior disorder and Parkinsonian motor signs suggests prodromal neurodegeneration in 22q11 deletion syndrome

Hyposmia, symptoms of REM sleep behavior disorder and Parkinsonian motor signs suggests prodromal neurodegeneration in 22q11 deletion syndrome

... This is a repository copy of Hyposmia, symptoms of REM sleep behavior disorder and Parkinsonian motor signs suggests prodromal neurodegeneration in 22q11 deletion syndrome.. White Rose R[r] ... See full document

16

Fregoli syndrome in course of infection-related delirium. A case report

Fregoli syndrome in course of infection-related delirium. A case report

... In patients with delirium, exposure to severe infectious states in- duce different degrees of inflammation according to the baseline status of the peripheral ChE activity, suggesting that delirium is associated ... See full document

6

Chromosome 22q11 Deletion in Patients With Ventricular Septal Defect: Frequency and Associated Cardiovascular Anomalies

Chromosome 22q11 Deletion in Patients With Ventricular Septal Defect: Frequency and Associated Cardiovascular Anomalies

... series, patients with a right aortic arch and/or an abnormal aortic arch branching pat- tern were significantly more likely to have a chromo- some 22q11 deletion than those with a normally branching ... See full document

7

Breast cancer in patients with Li–Fraumeni syndrome – a case-series study and review of literature

Breast cancer in patients with Li–Fraumeni syndrome – a case-series study and review of literature

... every 2 years), and melanoma (annual dermatologic exam) along with a general assessment (physical exam every 3–4 ...40 patients underwent surveillance and 49 declined surveillance (however, 19 ... See full document

9

Social cognition in patients with schizophrenia

Social cognition in patients with schizophrenia

... L’analisi dei dati è stata effettuata considerando la differenza tra i gruppi (Gruppo di Controllo m età = 36,33 vs. Gruppo Sperimenta- le m età = 36,16): la differenza nel[r] ... See full document

6

Cardiovascular Anomalies in Patients Diagnosed With a Chromosome 22q11 Deletion Beyond 6 Months of Age

Cardiovascular Anomalies in Patients Diagnosed With a Chromosome 22q11 Deletion Beyond 6 Months of Age

... (38%) patients: 3 with a vascular ring formed by a right aortic arch with an aberrant left subclavian artery and left-sided ligamentum arteriosum, 3 with a right aortic arch with mirror-image branching of the ... See full document

6

Blood brain barrier regulation in psychiatric disorders

Blood brain barrier regulation in psychiatric disorders

... in schizophrenia [108,109], although another study found no di ff er- ences between patients and controls from a total of 63 patients with chronic schizophrenia ...in schizophrenia [111] ... See full document

14

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype

... microdeletion syndrome (MIM613026) is a clinically recognisable condition that has been recently identified by molecular karyotyping ...we report the first case of 19q13.11 microdeletion ... See full document

7

Show all 10000 documents...