Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability
Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability
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DOI:
10.1111/jir.12117
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发表时间:
2014-10-01
影响因子:
3.6
通讯作者:
Curfs, L. M. G.
中科院分区:
文献类型:
--
作者:
Evers, L. J. M.;van Amelsvoort, T. A. M. J.;Curfs, L. M. G.
Background22q11 deletion syndrome (22q11DS) is associated with mild or borderline intellectual disability (ID). There are hardly any reports on subjects with 22q11DS with moderate or severe ID, and therefore its behavioural and psychiatric characteristics are unknown.MethodWe describe behavioural and psychiatric characteristics of 33 adults with 22q11DS and a Full-Scale IQ (FSIQ) below 55. Participants were divided into two groups: one group having a FSIQ55 caused by intellectual decline (n=21) and one group with a FSIQ55 who had always functioned at this level (n=12).ResultsHigh scores on psychopathology sub-scales were found for both subgroups. 22q11DS patients with intellectual decline showed higher rates of co-morbid psychopathology, particularly psychosis. Furthermore, psychosis and intellectual decline were positive correlated.ConclusionThis is the first report addressing adult patients with 22q11DS and moderate to severe ID. Overall we found high levels of psychopathology with higher scores of psychopathology in the intellectual decline group. Life time psychosis seems to be related to deterioration.