scholarly journals “An Unusual Case Study of Disguised Signatures Executed Freely by Modifying Characters on Agreement of Sell”

2022 ◽  
Vol 10 (1) ◽  
pp. 353-358
Author(s):  
Dr. Ravindra Sharma
Keyword(s):  
Unusual Case ◽  
Document Examiners

Abstract: Disguised writing is any deliberate attempt to alter one’s handwriting characteristics to prevent recognition. Disguised writings throw several problems for document examiners when dealing with various disputed documents. The handwriting characteristics are subdued in the subconscious mind of an individual thus, cannot be altered or disguised easily. The present write up is to unfold the journey of FDE, examining writings or signatures having wilful modification for the purpose of concealing his/her identity. In this case, a person attempts to disguise his signatures on agreement of sell with an intention of denying the signatures at a laterstage. Keywords: Disguised writing, handwriting characteristics, signatures, freely executed, modification etc.

scholarly journals Endovascular Management of Middle Aortic Syndrome Presenting with Uncontrolled Hypertension

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Owen S. Glotzer ◽  
Kathryn Bowser ◽  
F. Todd Harad ◽  
Sandra Weiss
Keyword(s):  
Open Surgery ◽  
Unusual Case ◽  
Case Series ◽  
Uncontrolled Hypertension ◽  
Endovascular Management ◽  
Vascular Disorder ◽  
Middle Aortic Syndrome ◽  
Surgical Bypass ◽  
Endovascular Approach

Middle Aortic Syndrome is a rare vascular disorder consisting of narrowing or stenosis of the distal thoracic or abdominal aorta. It is described in the literature in the form of case studies and case series. The authors present an unusual case of Middle Aortic Syndrome attributed to Takayasu’s arteritis in a 60-year-old female who presented to the emergency department with uncontrolled hypertension. Traditional intervention involves open surgical bypass. This case study reviews the published literature on this rare syndrome and illustrates a successful alternative to open surgery through an endovascular approach.

Gradual evolution of male genitalia in a sibling species complex of millipedes (Diplopoda : Spirobolida : Rhinocricidae : Anadenobolus)

2003 ◽  
Vol 17 (6) ◽  
pp. 711 ◽  
Author(s):  
Jason E. Bond ◽  
David A. Beamer ◽  
Marshal C. Hedin ◽  
Petra Sierwald
Keyword(s):  
Male Genitalia ◽  
Species Complex ◽  
Unusual Case ◽  
Incomplete Lineage Sorting ◽  
Rapid Change ◽  
Nuclear Gene ◽  
Lineage Sorting ◽  
Gradual Evolution ◽  
Copulatory Structure

Jamaican millipedes in the Anadenobolus species complex provide an unusual case study of arthropods having undergone speciation in the absence of conspicuous divergence of male genitalia. Using landmark-based morphometrics, we examined shape deformation of the male anterior copulatory device in three genetically divergent yet morphologically cryptic species. A multivariate analysis of variance and relative warp analysis of nonuniform components show that although male genitalic shape is statistically different among species, many specimens are 'misplaced' in morphological space, perhaps consistent with a condition analogous to incomplete lineage sorting. A simulation of neutral nuclear gene coalescence suggests that such incomplete sorting is expected, given the depth of mtDNA divergences observed across species. The pronounced contrast between deep molecular v. incomplete genitalic divergence is at odds with the paradigm of selection-driven rapid change in male copulatory structure during arthropod speciation. Alternatively, we suggest that male genitalic divergence is evolving neutrally or in concert with other components of the genome (pleiotropy). Although we recognise the empirical validity of rapid genitalic divergence via sexual selection or sexual conflict, such models must be empirically tested using multiple lines of evidence. Accepting the rapid and divergent hypothesis without such multiple evidence scrutiny may result in a gross underestimation of evolutionary diversity and, subsequently, the misinterpretation of processes shaping genitalic change.

Fetus in Fetu: An Unusual Case Study for the Neonatal Nurse Practitioner

2011 ◽  
Vol 30 (5) ◽  
pp. 313-319
Author(s):  
Natalie Mercy
Keyword(s):  
Neonatal Intensive Care ◽  
Unusual Case ◽  
Abdominal Distension ◽  
Final Diagnosis ◽  
Fetus In Fetu ◽  
Intensive Care Unit Team ◽  
Abdominal Masses ◽  
Unusual Occurrence ◽  
Severe Coagulopathy

Fetus in fetu is an extremely unusual occurrence where a rare congenital tumor containing a vertebral axis, often containing parts of other organs or limbs, is identified. Normally identified in the newborn period, the size and location of the mass may result in significant multiorgan compromise. This article presents the challenges encountered by the neonatal intensive care unit team in providing care for a late preterm female infant presenting with gross abdominal distension. Description of the case includes preoperative management along with management of severe coagulopathy and hemorrhage that arose during the intraoperative and postsurgical course of care. A brief overview of abdominal masses in the newborn is presented. The importance in determining the final diagnosis of fetus in fetu and its differentiation from teratoma is discussed.

Case Study - An Unusual Case of Bleeding

2018 ◽  
Vol 113 (Supplement) ◽  
pp. S1149
Author(s):  
Ian Turner ◽  
Priya Acharya
Keyword(s):  
Unusual Case

Orestes in Southern California: A Forensic Case of Matricide

1996 ◽  
Vol 24 (1) ◽  
pp. 77-102 ◽  
Author(s):  
J. Reid Meloy
Keyword(s):  
Mental Illness ◽  
Schizoaffective Disorder ◽  
Southern California ◽  
Unusual Case ◽  
Real Life ◽  
Developmental Trauma ◽  
Forensic Case

The author presents an unusual case study of matricide, one in which the perpetrator, a 33-year-old poet and actor, acted out the role of Orestes in real life. The biogenic basis of his mental illness, schizoaffective disorder, was exacerbated by a developmental trauma—the loss of his father to polio and of his mother to psychosis—as a toddler. The only psychotic avenue to his masculine identification and separation from his mother as an adult was murder.

scholarly journals Pigmented Free-Floating Posterior Vitreous Cyst

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Claudia Bruè ◽  
Cesare Mariotti ◽  
Edoardo De Franco ◽  
Nicola De Franco ◽  
Alfonso Giovannini
Keyword(s):  
Unusual Case ◽  
Color Doppler ◽  
Color Doppler Ultrasound ◽  
Fundus Examination ◽  
Pigmented Lesion ◽  
Ocular Disorders ◽  
Vitreous Cyst ◽  
The Right ◽  
Internal Reflectivity

Vitreous cysts are very rare ocular malformations. In this observational case study, we report on an unusual case of a pigmented free-floating vitreous cyst and discuss its differential diagnosis. A 14-year-old male was referred to ophthalmology for a pigmented lesion in his left eye. He complained of an intermittent floater in the left eye. Visual acuity was 20/20 in the right eye and 20/40 in the left eye. Fundus examination was unremarkable bilaterally, except for a piece of brownish oval material floating in the vitreous in the left eye. He had received a knock on the left side of his head a few days before the visual discomfort of the left eye. Real-time ultrasound of the left eye detected a piece of hyperechogenic spherical material with no internal reflectivity, floating in the middle of the vitreous. The first use of color Doppler ultrasound in this context indicated no arterial flow, ruling out the presence of a persistent hyaloid artery. Intraocular cysts are rare ocular disorders, which have been divided into clear and pigmented cysts, and into those that occupy the anterior chamber, the retrolental space, and the vitreous cavity. This last is extremely rare. We describe such a case.

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