Shruti Thakur

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The morphogenesis of the pancreas is a complex process having a very low frequency of anatomic variation. The congenital anomalies are rare. Complete pancreatic and ventral pancreatic agenesis are incompatible with life. Dorsal pancreatic agenesis is exceedingly rare with less than 100 cases reported in the world literature. Patients with this anomaly may(More)
In the present work, a hybrid hierarchical framework for classification of breast density using digitized film screen mammograms has been proposed. For designing of an efficient classification framework 480 MLO view digitized screen film mammographic images are taken from DDSM dataset. The ROIs of fixed size i.e. 128 × 128 pixels are cropped from the center(More)
Bacteriocins are antimicrobial peptides which are ribosomally synthesized by mainly all bacterial species. LABs (lactic acid bacteria) are a diverse group of bacteria that include around 20 genera of various species. Though LABs have a tremendous potential for production of anti-microbial peptides, this group of bacteria is still underexplored for(More)
A 35-year-old woman presented with generalized abdominal pain for the past 2 years. The pain was intermittent and moderate in intensity. There was no anorexia, vomiting, or fever. Her bladder and bowel habits as well as physical and abdominal examination were normal. The routine blood and urine tests were also unremarkable. The ultrasound done as a(More)
Craniosynostosis means premature closure of calvarial sutures. It may be primary or secondary. The patient presents with unexplained neuropsychological impairment and radiological imaging clinches the diagnosis. We present a case of 31-year-old female having primary isolated craniosynostosis who survived into adulthood without any surgical intervention. The(More)
Disseminated cysticercosis is a rare complication characterized by extensive dissemination of larvae (Cysticercus cellulosae) of Taenia solium throughout the human body involving brain, subcutaneous tissue, skeletal muscles and other organs. The symptoms depend upon the parasite burden, its location, stage of cyst evolution and host immunity. We report a(More)
Intracranial lipomas are congenital malformations. These uncommon lesions have an incidence of 0.1 to 1.7% of all intracranial tumors. Most cases are located at midline and 5% are along the sylvian fissures. If symptomatic, seizures are the most common symptom. These tumors are slow growing and have favorable outcome. We report a case of a 25-year-old man(More)
Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland syndrome, is a rare syndrome with unknown etiology. The syndrome is characterized by a triad of unique cutaneous, ocular, and central nervous system (CNS) manifestations. The cutaneous hallmark, nevus psiloliparus (NP), along with overlying alopecia is a constant feature. Choristoma of the(More)