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Literature DB >> 15967641

Basal ganglia calcification and psychosis in 22q11.2 deletion syndrome.

M Sieberer¹, H Haltenhof, B Haubitz, B Pabst, K Miller, P Garlipp.

Abstract

Intracerebral calcifications are a facultative symptom of hypoparathyreoidism in 22q11.2 deletion syndrome (22qDS). We describe a patient with 22qDS, basal ganglia calcification (BGC) and psychotic symptoms and discuss the etiological connection of BGC with psychiatric symptoms. Future work needs to determine the prevalence of BGC in 22qDS and psychiatric disorders.

Entities: Disease Species

Mesh：

Year: 2005 PMID： 15967641 DOI： 10.1016/j.eurpsy.2005.04.002

Source DB: PubMed Journal: Eur Psychiatry ISSN： 0924-9338 Impact factor: 5.361

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Cited

9 in total

1. Commentary on Treatment Resistant Psychosis in an adolescent with scoliosis and a history of early feeding difficulties.

Authors: Andrea Stachon
Journal: J Can Acad Child Adolesc Psychiatry Date: 2007-02

Review 2. Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series.

Authors: Nancy J Butcher; Erik Boot; Anthony E Lang; Danielle Andrade; Jacob Vorstman; Donna McDonald-McGinn; Anne S Bassett
Journal: Am J Med Genet A Date: 2018-05-19 Impact factor: 2.802

3. Vitamin D deficiency, behavioral atypicality, anxiety and depression in children with chromosome 22q11.2 deletion syndrome.

Authors: L Kelley; A F P Sanders; E A Beaton
Journal: J Dev Orig Health Dis Date: 2016-12 Impact factor: 2.401

Basal ganglia calcification and psychosis in 22q11.2 deletion syndrome.

1. Commentary on Treatment Resistant Psychosis in an adolescent with scoliosis and a history of early feeding difficulties.

Review 2. Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series.

3. Vitamin D deficiency, behavioral atypicality, anxiety and depression in children with chromosome 22q11.2 deletion syndrome.

Review 4. Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients.

5. Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.

6. An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch.

7. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.

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

9. Two cases of chromosome 22q11.2 deletion syndrome diagnosed in 12-year-old boys with hypocalcemic seizures.