Relationship of birth season to clinical features, family history, and obstetric complications in schizophrenia

The early observations of those who first described babies with pyloric stenosis (PS) are used as a backdrop for the development of the Inherited Primary Hyperacidity theory of cause. Those early truths, uncomplicated by modern technology, have acted as a springboard for pathogenesis. Hyperacidity, male predominance, family history, self-cure, enhanced appetite, and time-sensitive presentation were all well known to the early pioneers. Any system of pathogenesis must explain all these clinical features. The Inherited Primary Hyperacidity theory does this and is a credible explanation for all the clinical features established by these early pioneers. The evidence which supports a delay in maturation of the negative feedback between gastrin and gastric acidity is presented. Such a phenomenon further supports the Primary Hyperacidity theory.

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Acne:Clinico-Epidemiological Study In DermatologyVenereology Outpatient Clinic Of Dr. M. Djamil Hospital Padang During January 2016 – December 2018

International Journal of PharmTech Research ◽

10.20902/ijptr.2019.130403 ◽

2020 ◽

Vol 13 (4) ◽

pp. 325-328

Author(s):

Satya Wydya Yenny

Keyword(s):

Retrospective Study ◽

Family History ◽

Epidemiological Study ◽

Clinical Features ◽

Outpatient Clinic ◽

Medical Records ◽

Skin Disorder ◽

Epidemiological Data ◽

Common Type ◽

History Of

Although acne is usually recognized as an adolescent skin disorder, the prevalence of adults with acne is increasing. The clinical and epidemiological data of acne were evaluated with a view to establishing possible contributing etiological factors and observing whether clinical features differ from adolescent acne. Division of Dermatology and Venereology Outpatient Clinic Dr. M. Djamil hospital padang during January 2016 until December 2018.Retrospective study performed in Medical Cosmetic Division of Dermatology and Venereology Outpatient Clinic Dr. M. Djamil hospital padang during January 2016 until December 2018. Data was taken from medical records. Out of 224 patients included in the study 54.01% were women and 45.98 % were men. Majority of the patients had comedonal acne (45.53 %), whereas nodulocystic was the least common (13.39%). Most common predominant site of involvement was cheek (44.20 %), followed by chin (25.45 %), and mandibular area (14.58 %). Family history of acne was present in 57.70 %. Scarring was observed in a 39.2 %. Acne is predominant in women, with the most commonly involved of the cheeks, with the most common type was comedones type.

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632 Family History of Children Diagnosed with Obstructive Sleep Apnea

SLEEP ◽

10.1093/sleep/zsab072.630 ◽

2021 ◽

Vol 44 (Supplement_2) ◽

pp. A248-A248

Author(s):

Kristi Porterfield-Pruss ◽

Denise Willis ◽

Beverly Spray ◽

Supriya Jambhekar

Keyword(s):

Family History ◽

Family Members ◽

Biological Father ◽

Medical Problems ◽

Obstructive Sleep ◽

Familial Association ◽

History Of ◽

The Mean ◽

Relationship Of ◽

The Relationship

Abstract Introduction Limited evidence suggests a familial association of OSA. It is not known how often children who require positive airway pressure (PAP) devices have a family member with OSA or that requires PAP. It is felt that PAP adherence in children is affected by PAP adherence in parents. We wanted to explore the relationship of OSA in children requiring PAP to OSA in immediate family members as well as the association of obesity and adherence between children and family members. Methods Caregivers of children who utilize PAP devices at home were invited to complete an electronic questionnaire regarding family history of OSA. Descriptive statistics were utilized to summarize results. Results The study was completed by 75 participants. The majority of children were male (64%, 48/75), black (47%, 35/75) and non-Hispanic (88%, 66/75). The mean age was 11.8 years (median 13) and mean BMI was 32.8 (median 29.8). The mean AHI on the diagnostic polysomnogram was 28.4 events per hour (median 15.3). Mean adherence to PAP > 4 hours per night was 56.5 (Median 68.2). Most, 87% (65/75), have other underlying medical problems. Twenty-four percent (18/75) have a biological father with OSA of whom 61% (11/18) are considered moderately/extremely obese. Of mothers, 13% (10/75) have OSA and 70% (7/10) are obese. Overall, 29% (22/75) had either a paternal (11%, 8/75) or maternal (19%, 14/75) grandfather with OSA of which 36% (8/22) are obese. For grandmothers, 31% (23/75) have OSA and 22% (5/23) are obese with more being paternal (19%, 14/75) compared to maternal (12%, 9/75). Of the 73 total family members reported to have OSA, 86% (63/73) use PAP and most (65%, 41/63) use it for > 4 hours every night. Few participants had siblings with OSA. Conclusion There were more fathers with OSA than mothers, but mothers were reported to be obese more often. Grandparents were reported to have OSA but were reported to be obese less often than parents. Maternal grandparents with OSA were reported to be obese more than paternal grandparents. The majority of family members with OSA who use CPAP report nightly use. Support (if any):

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The Association Between Triple X and Psychosis

The British Journal of Psychiatry ◽

10.1192/bjp.160.4.554 ◽

1992 ◽

Vol 160 (4) ◽

pp. 554-557 ◽

Cited By ~ 10

Author(s):

Wendy J. Woodhouse ◽

Anthony J. Holland ◽

Greg McLean ◽

Adrianne M. Reveley

Keyword(s):

British Journal ◽

Family History ◽

Psychiatric Disorder ◽

Obstetric Complications ◽

Psychiatric Practice ◽

Psychotic Illness ◽

Chromosome Anomalies ◽

Eeg Abnormalities ◽

Management Problems ◽

History Of

Two cases of psychotic illness in association with the karyotype triple X showed specific diagnostic and management problems as well as obstetric complications, EEG abnormalities, and lack of a family history of psychiatric disorder. Routine karyotyping during the investigation of psychosis is becoming relevant to psychiatric practice as research reports increasingly feature genetic and chromosome anomalies in association with schizophrenic psychoses.British Journal of Psychiatry (1992), 160, 554–557

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Maternal infectious diseases during pregnancy and obstetric complications in the etiology of distinct subtypes of schizophrenia: further evidence from maternal hospital records

European Psychiatry ◽

10.1016/0924-9338(96)80332-4 ◽

1995 ◽

Vol 10 (7) ◽

pp. 326-330 ◽

Cited By ~ 10

Author(s):

E Franzek ◽

G Stöber

Keyword(s):

Infectious Diseases ◽

Maternity Hospital ◽

Obstetric Complications ◽

Perinatal Complications ◽

Hospital Records ◽

Maternal Recall ◽

Genetic Loading ◽

Relationship Of ◽

The Relationship ◽

Good Agreement

SummaryOn the basis of 24 maternity hospital records, the current study investigated the validity of maternal recall and the relationship of maternal infections during pregnancy and obstetric complications (OCs) to different diagnostic subgroups of endogenous psychoses on which we reported previously in this journal. Maternal recall showed good agreement to maternity hospital records in the Lewis and Murray scale (ϑ = 0.74). With regard to infectious diseases during pregnancy maternal recall and records showed a weaker, but also good correlation (ϑ = 0.18). Psychoses with low genetic loading had more OCs than psychoses with high genetic loading. Maternal infectious diseases, especially during the fourth or fifth month of gestation, were significantly allocated to Leonhard's systematic schizophrenias. Data from maternity hospital records support our report that infectious diseases during midgestation and further perinatal complications seem to be important etiologic factors in systematic forms of schizophrenia without marked familial loading.

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Family History of Schizophrenia and the Relationship of Stress to Symptoms: Preliminary Findings

Australian & New Zealand Journal of Psychiatry ◽

10.1046/j.1440-1614.2001.00876.x ◽

2001 ◽

Vol 35 (2) ◽

pp. 217-223 ◽

Cited By ~ 15

Author(s):

Ross M. G. Norman ◽

Ashok K. Malla

Keyword(s):

Family History ◽

Negative Affect ◽

Negative Symptoms ◽

Positive Family History ◽

Positive Symptoms ◽

Daily Stressors ◽

Schizophrenic Patients ◽

History Of ◽

Relationship Of ◽

The Relationship

Objective: It has been hypothesized that patients with a diagnosis of schizophrenia who have a positive family history for schizophrenia will show greater reactivity of their symptoms to increasing levels of stress or negative affect than will patients without such a family history. In the past this hypothesis has only been tested through manipulations of negative affect in laboratory settings. In this paper we test this hypothesis using longitudinal clinical data. Method: Data were derived from an earlier longitudinal study using monthly assessments of daily stressors (Hassles Scale) and symptom measures (the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Negative Symptoms). We compared longitudinal stress to symptom relations in 12 patients with schizophrenia for whom a positive family history of schizophrenia could be identified with 12 matched schizophrenic patients without any known family history of psychiatric illness. Results: There was evidence that patients with a family history of schizophrenia demonstrated a stronger relation between stress and total score on the Scale for the Assessment of Positive Symptoms. This difference appears to have primarily reflected a greater reactivity to stress of reality distortion symptoms in the positive family history group. The two groups did not differ in apparent reactivity to stress of the disorganization and psychomotor poverty dimensions of symptomatology. Conclusions: The results of this study provide support from a naturalistic, longitudinal clinical study for the hypothesis that reactivity to stress of some symptoms of schizophrenia may vary as a function of family history of the disorder.

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