Mosaic Turner syndrome associated with schizophrenia.

Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide. Most Turner females had a 45,X monosomy, whereas the majority of comorbidity between Turner syndrome and schizophrenia had a mosaic karyotype (45,X/46,XX). We present a case of a 21-year-old woman with Turner syndrome, mosaic karyotype (45,X/46,XX), showing mental retardation, hypothyroidism, and schizophrenia. HOPA gene within Xq13 is related to mental retardation, hypothyroidism, and schizophrenia. Our case may be a potential clue which supports the hypothesis for involvement of genes on X chromosome in development of schizophrenia. Further studies including comorbid cases reports are need in order to discern the cause of schizophrenia in patients having Turner syndrome.

Introduction

Turner syndrome (TS) is relatively well-known sex chromosomal disorder that occurs in about 1/2,500 live newborn female1). TS is genetically caused by 45,X monosomy (60%), 45,X/46,XX mosaicism (30%), or other structural abnormality of X chromosome (10%). It is well known that TS individuals usually are affected 3 somatic systems of skeletal, reproductive, and lymphatic. The specific neuropsychological deficits associated with TS include mild mental retardation, attentional problems, memory impairments, visuospatial processing problems, deficits in fear recognition, anxiety, impairments in social cognition, and motor functioning problems2).

Psychosis is relatively rare in TS female, but some authors have hypothesized that psychosis can be associated with TS3). No defined psychiatric condition has been traditionally related to TS, and TS is not mentioned in DSM-IV (Diagnostic and Statistical Manual of Mental disorders, 4th edition). Less is known about the development of psychosis in female TS.

Here, we report a sporadic case of a young woman with mosaic TS who developed psychosis diagnosed as schizophrenia.

Case report

A 21-year-old woman with TS was admitted because of auditory hallucinations and altered behavior for last 2 months. At the age of 13 years, she was first diagnosed with TS, mosaic karyotype 45,X/46,XX, combined by central obesity, hyperlipidemia, and type 2 diabetes mellitus. Also, she had been diagnosed concomitant with idiopathic central diabetes insipidus presenting polyuria (4 L/day) and polydipsia (4-5 L/day) for 1 year4). A water deprivation test showed central diabetes insipidus, and the initial finding of sellar magnetic resonance imaging (MRI) showed a thickening of the pituitary stalk with normal high signal intensity in the posterior pituitary gland. She had been managed with metformin, estrogen, and oral 1-deamino-8-D-arginine vasopressin, to which she had maintained well with about 2 L of daily urine volume. Follow-up MRI imaging had taken 2 years later demonstrated a nearly normal pituitary stalk thickness4).

At the age of 14 years, she had been treated with additional drug, levothyroxine due to Hashimoto's thyroiditis induced primary hypothyroidism. At the age of 18 years, her intelligence quotient (IQ) score was 52, suggestive of mild mental retardation, while her social quotient was at a level of 8 years. After graduated high school, she entered a vocational school for mentally disabled people. In school, she volunteered for a class senator, attended school punctually at any situation. She actively talked in school, so she earned the nickname 'radio'. She was active and honest daughter who lives with parents and younger brother. There was no history of alcohol or drug abuse. None of family members had psychiatric illness or mental retardation.

Before 2 months prior to admission, she suddenly avoided to talk and go to school and redundantly wanted to sleep without social interaction. She developed excessive daytime sleepiness and bizarre behavior with auditory hallucination 2 weeks ago. After taking oral medication prescribed by a psychiatric clinic, her symptoms including insomnia, visual and auditory hallucination were exacerbated. On mental status examination at admission, she showed poverty of speech, dysarthria, anxious mood, auditory hallucination, visual hallucination, persecutory delusion, social withdrawal, soliloquy, avolition, and aggressive behavior. Her orientation was intact for time, place, and person.

At admission to our hospital, the patient's height was 145 cm (percentile<3th) and her weight was 51.5 kg (25thcubitus valgus were observed. Neurological examinations were normal. Laboratory findings revealed serum glucose, 107 mg/dL (normal, 70-100 mg/dL); glycosylated hemoglobin, 6.8% (normal, 4.0%-6.0%); normal free T4 level, 1.96 ng/dL (normal, 0.80-1.90 ng/dL); and thyroid-stimulating hormone, 0.80 mIU/L (normal : 0.17-5.65 mIU/L); sodium, 133 mEq/L (normal, 133-145 mEq/L); potassium, 3.8 mEq/L (normal, 3.5-5.5 mEq/L); chloride 96, mEq/L (normal, 95-110 mEq/L); serum osmolarity, 280 mOsm/kg (normal, 288-302 mOsm/kg); urine osmolarity, 464 mOsm/kg (normal, 300-900 mOsm/kg). The last follow-up MRI showed no significant interval change of pituitary stalk thickening compared to previous MRI finding and no abnormal pituitary mass or brain parenchymal abnormality. After diagnosed as having psychotic disorder, she was started on oral ziprasidone, which was gradually increased. She showed significant improvement after 1 month, but her symptoms were waxing and waning without full remission. She is under regular follow-up for the last 10 months.

Discussion

The majority of individuals with TS are known to have normal intelligence with normal verbal abilities5). On the other hand, several studies have revealed that TS patients may show decreased full-scale IQ, and have selective impairments with regard to visuo-spatial processing and visuo-perceptual skills2). The risk of memory and attention problems and the risk of developing autism and attention deficit hyperactivity disorder in TS are higher than in the normal population6,7). Furthermore neuroanatomical imaging provided evidence of abnormalities in several brain structures, including the parietal lobe, amygdala, hippocampus, and orbito-frontal cortex8).

Schizophrenia is a complex genetic disorder with a prevalence of about 1%9). Genetic factors play an important role in the developing schizophrenia. The risk of schizophrenia is 3 times higher in people with mild learning disability than in the general population and chromosomal abnormalities are increased. In general, TS is found about three times more often in female schizophrenics than in the general female population3,10). Previous researches studying sex chromosome abnormalities in schizophrenic subjects have investigated the role of extra-X chromosome in Klinefelter syndrome (47,XXY) or triple X (47,XXX).

Recently the hypothesis of a locus within the pseudoautosomal region of the X chromosome conferring susceptibility to schizophrenia has been studied. DeLisi et al.11) reported that neuropsychiatric findings of XXY karyotype individuals with schizophrenia result from genes within the pseudoautosomal region in the X chromosome and tend to avoid normal extra-X chromosome inactivation. These regions may produce their gene products in excess, influencing normal brain growth and differentiation. On the other hand nonpseudoautosomal regions of the X chromosome, mapping to a locus on Xp21, have been associated with the development of schizophrenia12).

TS may lead to an increased risk for schizophrenia. To our knowledge, there are few published cases of schizophrenia in TS individuals due to the rarity of both disorders, total 20 cases have been described in the English literature10,13). Interestingly, most TS females had a 45,X nonmosaic karyotype, whereas the majority (19/20) of comorbidity between TS and schizophrenia had a mosaic karyotype (45,X/46,XX). Thus, it has been suggested that the potential of gene dose-effect might be associated with abnormal expression of an X chromosome gene product, which have susceptibility for schizophrenia in TS10).

Recently Roser and Kawohl13) published a case report on TS, schizophrenia, mental retardation, and hypothyroidism associated with polymorphism of the human opposite paired (HOPA) gene, located on Xq13. The HOPA gene is associated with mental retardation, thyroid dysfunction, and neuropsychiatric disorders. HOPA gene product belongs to the thyroid receptor associated protein that codes for a coactivators for thyroid hormone receptor14). Because the HOPA gene is expressed throughout the central nervous system in the period of fetal development, the abnormality in the HOPA gene is hypothesized to raise risk for schizophrenia15). Also, an association between the HOPA polymorphism and mental retardation was reported15,16). The Xq13 region, including the X inactivation center and a gene escaping X inactivation, may contribute to the X inactivation process in addition to the pathogenesis of schizophrenia in TS17).

The findings for our TS patient, who had the mosaic karyotype, were very similar to the clinical findings, such as mental retardation, schizophrenia, and hypothyroidism in the case reported by Roser and Kawohl13). Hypothyroidism in our case was caused by Hashimoto thyroiditis. Several studies reveled that schizophrenia is linked with some autoimmune diseases, especially autoimmune thyroid disease, type 1 diabetes, celiac disease, rheumatoid arthritis16,18). She might be the similar case of comorbid TS and schizophrenia, mental retardation, hypothyroidism, which speculated the genetic possibility such as the HOPA gene on the X chromosome might be involved in the development of schizophrenia.

In Korea, only two cases with both chronic psychosis and TS were reported19,20). Both patients had the mosaic karyotype of 45,X/46,XXp- without mental retardation as well.

Further studies, including comorbid case reports are needed in order to discern the pathogenesis of schizophrenia in TS. It is important for practitioners to understand the clinical spectrum and the natural courses, including the development of schizophrenia, in mosaic TS.