EXCESSIVE PRODUCT TRADING: A RARE FORM OF BEHAVIORAL ADDICTION

Morgagni hernia is a rare form of diaphragmatic hernia. It is a congenital defect of the diaphragm, often asymptomatic in adulthood and thus usually found only incidentally. Its treatment is predominantly surgical. This article presents three case reports of patients operated in our department.

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Diagnosis and Ablation of Fascicular Tachycardia

Asia Pacific Cardiology ◽

10.15420/apc.2011:3:1:67 ◽

2011 ◽

Vol 3 (1) ◽

pp. 67

Author(s):

Akihiko Nogami ◽

Keyword(s):

Ventricular Tachycardia ◽

Right Bundle Branch Block ◽

Axis Deviation ◽

Exit Site ◽

Rare Form ◽

Bundle Branch Block ◽

Diagnosis And Therapy ◽

Narrow Qrs ◽

Left Posterior ◽

Qrs Morphology

Verapamil-sensitive fascicular ventricular tachycardia (VT) is the most common form of idiopathic left VT. According to the QRS morphology and the successful ablation site, left fascicular VT can be classified into three subgroups: left posterior fascicular VT, whose QRS morphology shows right bundle branch block (RBBB) configuration and superior axis (common form); left anterior fascicular VT, whose QRS morphology shows RBBB configuration and right-axis deviation (uncommon form), and upper septal fascicular VT, whose QRS morphology shows narrow QRS configuration and normal or right-axis deviation (rare form). Posterior and anterior fascicular VT can be successfully ablated at the posterior or anterior mid-septum with a diastolic Purkinje potential during VT or at the VT exit site with a fused pre-systolic Purkinje potential. Upper septal fascicular VT can also be ablated at the site with diastolic Purkinje potential at the upper septum. Recognition of the heterogeneity of this VT and its unique characteristics should facilitate appropriate diagnosis and therapy.

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Cystic struma ovarii, a rare form of ovarian tumor – a case report, and review of the literature

Orvosi Hetilap ◽

10.1556/oh.2007.28202 ◽

2007 ◽

Vol 148 (48) ◽

pp. 2285-2287 ◽

Cited By ~ 1

Author(s):

Gabriella Östör ◽

Ildikó Tóth ◽

Zsuzsanna Hrubyné Tóth ◽

Sándor Bazsa

Keyword(s):

Case Report ◽

Ovarian Tumor ◽

Ca 125 ◽

Struma Ovarii ◽

Review Of The Literature ◽

Rare Form

Az ovarialis strumák a petefészek-teratomák kevesebb mint 3%-át adják. Megjelenhet bennük a pajzsmirigy szinte minden betegsége, és előfordulhat malignitás is. A szerzők esetében egy 31 éves nő bal oldali petefészekcisztáját távolították el, amely az ovariumcarcinoma klinikai tüneteit mutatta, úgymint nagy hasi térfoglalás, ascites, emelkedett szérum-CA 125-szint. A szövettani diagnózis benignus struma ovarii volt. A posztoperatív pajzsmirigyműködés normális maradt.

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Aspirine asthma in children - not a rare form of disease

SOVREMENNAYA PEDIATRIYA ◽

10.15574/sp.2015.72.99 ◽

2015 ◽

Vol 72 (8) ◽

pp. 99-106

Author(s):

Е.N. Оkhotnikova ◽

◽

L.V. Duda ◽

G.V. Shklyarska ◽

◽

...

Keyword(s):

Rare Form ◽

Asthma In Children

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Case of follow-up and successful surgical treatment rare form of subaortic membrane in infant

CHILDREN’S HEART AND VASCULAR DISEASES ◽

10.24022/1810-0686-2017-14-3-161-165 ◽

2017 ◽

Vol 14 (3) ◽

pp. 161-165

Author(s):

A.I. Kim ◽

Т.V. Rogova ◽

R.М. Кurganov ◽

Е.V. Kholmanskaya

Keyword(s):

Surgical Treatment ◽

Rare Form ◽

Subaortic Membrane

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A RARE FORM OF HYPOPHOSPHATEMIC RICKETS DUE TO MUTATIONS IN THE SLC34A3 GENE: DIAGNOSIS AND TREATMENT PECULIARITIES

PEDIATRIA Journal named after G N SPERANSKY ◽

10.24110/0031-403x-2018-97-6-69-73 ◽

2018 ◽

Vol 97 (6) ◽

pp. 69-73

Author(s):

E.A. Nikolaeva ◽

◽

S.Yu. Kuznetsova ◽

V.Yu. Voinova ◽

Yu.I. Davydova ◽

...

Keyword(s):

Diagnosis And Treatment ◽

Hypophosphatemic Rickets ◽

Rare Form ◽

Gene Diagnosis

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Binge Eating and Problem Gambling are Associated with Common and Distinct Deficits in Emotion Regulation among Community Women: Results from a Prospective Study

10.31234/osf.io/v9nbs ◽

2020 ◽

Author(s):

Sarah Farstad ◽

Kristin M. von Ranson

Keyword(s):

At Risk ◽

Emotion Regulation ◽

Binge Eating ◽

Problem Gambling ◽

Prospective Study ◽

Emotion Dysregulation ◽

Behavioral Addiction ◽

Negative Urgency ◽

Cross Sectional ◽

Severe Problem

To elucidate similarities and differences between binge eating and a behavioral addiction, this prospective study compared facets of emotion regulation that were associated with problem gambling, the only formally recognized behavioral addiction, and binge eating. Community-based women (N = 202) who engaged in at-risk binge eating (n = 79), at-risk gambling (n = 36), or both (n = 87) completed four online assessments over six months. Baseline and six-month surveys assessed self-reported emotion dysregulation (using the DERS and UPPS-P), binge eating (using the EDE-Q), and gambling (using the PGSI); abbreviated two- and four-month surveys assessed only binge eating and gambling. Binge eating and problem gambling were both associated with emotion dysregulation, and greater positive urgency was correlated with more severe problem gambling but less frequent binge eating. Negative urgency explained no unique variance in binge eating or problem gambling changes over time, once other facets of emotion dysregulation (i.e., positive urgency and facets assessed by the DERS) were included. Thus, previous cross-sectional research may have overestimated the association of negative urgency with both binge eating and problem gambling. Overall, these findings suggest that binge eating and problem gambling are associated with common as well as distinct emotion regulation deficits.

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Prenatal diagnosis of rare form chromosomal pathology: double aneuploidy

10.21516/2413-1458-2019-18-3-237-244 ◽

2019 ◽

Author(s):

L.A. Khlevnaya, S.A. Malova, L.I. Mitusova

Keyword(s):

Prenatal Diagnosis ◽

Clinical Manifestation ◽

Rare Form ◽

Chromosomal Disease ◽

Phenotypic Features ◽

Double Aneuploidy

The article represents the double aneuploidy, a rare form of chromosome pathology. 6 cases of double aneuploidy were diagnosed prenatally and 1 case was diagnosed postnatal. A variety of ultrasound signs is shown in this chromosomal pathology. The prevalence of phenotypic features of the chromosomal disease, which has the greatest clinical manifestation, was noted.

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