An Alleged Father's Family Medical History: An Introduction to the Nonidentifying Paternal Information Form

2014 ◽  
Vol 52 (3) ◽  
pp. 578-591
Author(s):  
Charisma J. Ross
2008 ◽  
Vol 18 (6) ◽  
pp. 433-439 ◽  
Author(s):  
Anneclaire J. de Roos ◽  
Glinda S. Cooper ◽  
Michael C. Alavanja ◽  
Dale P. Sandler

2012 ◽  
Vol 19 (2) ◽  
pp. e10-e14 ◽  
Author(s):  
P Pahwa ◽  
CP Karunanayake ◽  
L Hagel ◽  
JA Gjevre ◽  
D Rennie ◽  
...  

BACKGROUND: Increased daytime sleepiness is an important symptom of obstructive sleep apnea (OSA). OSA is frequently underdiagnosed, and the Epworth Sleepiness Scale (ESS) can be a useful tool in alerting physicians to a potential problem involving OSA.OBJECTIVE: To measure the prevalence and determinants of daytime sleepiness measured using the ESS in a rural community population.METHODS: A community survey was conducted to examine the risk factors associated with ESS in a rural population in 154 households comprising 283 adults. Questionnaire information was obtained regarding physical factors, social factors, general medical history, family medical history, ESS score, and self-reported height and weight. Multivariable binary logistic regression analysis based on the generalized estimating equations approach to account for clustering within households was used to predict the relationship between a binary ESS score outcome (normal or abnormal) and a set of explanatory variables.RESULTS: The population included 140 men (49.5%) and 143 women (50.5%) with an age range of 18 to 97 years (mean [± SD] 52.0±14.9 years). The data showed that 79.2% of the study participants had an ESS score in the normal range (0 to 10) and 20.8% had an ESS score >10, which is considered to be abnormal or high sleepiness. Multivariable regression analysis revealed that obesity was significantly associated with an abnormal or high sleepiness score on the ESS (OR 3.40 [95% CI 1.31 to 8.80).CONCLUSION: High levels of sleepiness in this population were common. Obesity was an important risk factor for high ESS score.


2020 ◽  
Vol 11 (3) ◽  
Author(s):  
Mostafa Vahedian ◽  
Amrollah Salimi ◽  
Omid Garkaz ◽  
Seyedeh Tasnim Abdi ◽  
Somayeh Donyadideh ◽  
...  

Background: Middle ear inflammation and fluid accumulation are one of the most common childhood diseases. Untreated or chronic ear inflammation can lead to more serious complications, including hearing loss, eardrum rupture, adhesive otitis media, tympanosclerosis, temporal bone necrosis, and cholesteatoma. Ventilation tube insertion is one of the best treatments to cure these diseases. Objectives: This aimed to observe children suffering from ear inflammation who were candidates for VT insertion surgery and study surgical complications. Methods: A historical cohort study was performed, and 205 VT surgeries were studied. Demographic information of children (like age, sex, and family medical history) was gathered through their medical records and probable complications, including otorrhea, tympanosclerosis, atrophy, and eardrum rupture were noticed through medical examinations and interviews. Data were analyzed using descriptive statistics, chi-square test, independent t-test, Fisher’s exact, and Mann-Whitney U-test. Results: The results showed that 57% of surgery cases were boys, and 43% were girls, both having no family medical history. Serous otitis with tonsillar hypertrophy was reported in 200 cases (97.6%), which had concurrent adenoidectomy or adenotonsillectomy. The frequency of otorrhea, tympanosclerosis, atrophy, perforation, and serous otitis recurrence was 2%, 12.2%, 6.8%, 1.5%, and 14.1%, respectively. Serous otitis recurrence was reported in 3.9% of cases with T-tube insertion. Conclusions: The findings of this study show no significant difference in surgical complications between the two groups of girls and boys. But studying the relationship between the age of patients and the timing of surgery shows that the mean age of girls is significantly higher.


2019 ◽  
Vol 25 (1) ◽  
pp. 5
Author(s):  
Xavier Lagarde ◽  
Mathilde Fenelon ◽  
Jean Christophe Fricain

Observation: A 19-week-old patient seen in an oral dermatology clinic had small labial commissures pits associated with auricular abnormalities. Similar clinical elements were found in the family medical history. A diagnosis of branchio-oto-renal syndrome (BOR) was quickly evoked. Commentary: BOR syndrome is a rare disease. This autosomal dominant pathology is characterized by facial lesions and renal abnormalities. Diagnosis is based on many clinical criteria. An optional genetic study can sometimes assist in diagnosis.


Author(s):  
Michael Snyder

When we visit the doctor, we are commonly asked to fill out a questionnaire about our family medical history, including major diseases such as cancer and heart disease experienced by our parents, siblings, and children. This is a rough way of gauging our risk...


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