Publications by authors named "Syed Maaz Tariq"

Article Synopsis
  • * A case involving an eight-year-old girl showed symptoms like short stature, abnormal teeth, fatigue, polydactyly (extra fingers), genu valgum (knock knees), and mild cardiomegaly (enlarged heart), which pointed to EVC.
  • * Diagnosis of EVC relies on detailed radiological tests, and managing the condition benefits from a collaborative approach involving multiple healthcare specialists.
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Maintenance therapies in multiple myeloma improve survival after induction treatment. This study characterizes the strategies for maintenance therapy being employed in currently enrolling clinical trials for patients with multiple myeloma and highlights how high-risk myeloma patients may be assigned to maintenance strategies incongruent with current US guidelines.

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Article Synopsis
  • Multiple myeloma (MM) is a type of cancer that is tough to cure and is related to bad habits like being overweight and not eating well.
  • This article talks about how being obese might increase the risk of getting MM and how it can affect the health of people who already have it.
  • It suggests that more research is needed to see if changing habits like diet and exercise can help prevent MM and improve life for those at risk.
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Pulmonary Langerhans cell histiocytosis (PLCH, pulmonary eosinophilic granuloma) is a rare disease of clonal dendritic cells that primarily affects adults who smoke cigarettes. PLCH association with other malignancies is rarely reported. Herein, an unusual case of PLCH is presented with synchronous lung adenocarcinoma.

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With the elderly population increasing in numbers, their demand of adequate medical and psychological care is also rising up. The key goal of promoting physical and mental health in elderly is maintenance of adequate health-related quality of life (QOL). A cross-sectional, descriptive study was conducted from December 2016 to February 2017 among 100 elderly living in nursing facilities and 100 in homes.

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Harlequin baby is rare and it is the most severe kind of congenital ichthyosis. It manifests as severely keratinized skin with an autosomal recessive inheritance. Incidence of this disease is 1 in 300,000 live births.

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Despite significant advancements, relapses, and persistent malignancies are still a major challenge faced by the oncologists. Immunotherapy has shown remarkable potential in induction of sustained remission in refractory malignancies. Chimeric antigen receptor T-cell (CAR-T) therapy is a newer treatment methodology approved by the Food and Drug Administration (FDA).

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In recent years, transcranial magnetic stimulation has become an area of interest in the field of neurosciences due to its ability to non-invasively induce sufficient electric current to depolarize superficial axons and networks in the cortex and can be used to explore brain functioning. Evidence shows that transcranial magnetic stimulation could be used as a diagnostic and therapeutic tool for various neurological and psychiatric illnesses. The aim of this review is to introduce the basics of this technology to the readers and to bring together an overview of some of its clinical applications investigated thus far.

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Pheochromocytoma, a rare tumour, arises mainly in the adrenal gland. It consists of chromaffin cells or sympathetic para-ganglia if extra-adrenal. It is an occurrence of rare nature with an incidence of two to eight cases per million annually.

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Article Synopsis
  • - Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndromes, which can lead to serious conditions like heart attacks and sudden death, and its causes and treatments are not well understood.
  • - A case study of a 42-year-old woman with vitamin B12 deficiency illustrates how SCAD can occur even in patients without typical heart disease risk factors, as she experienced chest pain and had an ECG indicating a heart attack.
  • - The cardiac catheterization revealed a significant dissection in the left anterior descending artery, which underscores the urgency and complexity of diagnosing SCAD.
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Cerebral air embolism (CAE) is a rare, avoidable and potentially fatal iatrogenic complication. Here, we report a case of CAE associated with a central venous catheter in the internal jugular vein that resulted in neurological deficits and generalised epileptic seizures. A 64-year-old man admitted for fasciotomy for compartment syndrome developed CAE with left-sided neurological deficits.

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Takayasu arteritis is an idiopathic chronic vasculitis that involves large blood vessels, including the aorta and its main branches. This disease presents typically as ischemia or aneurysms that could be prevented by timely diagnosis and vigilant management. We present here the case of a 19-year-old male who presented with a history of visual disturbance, chest pain, dizziness, and a feeble pulse.

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Tetralogy of Fallot (TOF) is the most common congenital heart disease (CHD) with an incidence of four in every 1000 live births in Pakistan. Classically, these children present with central cyanosis in early life; however, milder defects may remain asymptomatic for months or even years. We report a malnourished and anemic teenage male, who was admitted with shortness of breath, hemoptysis, fever, palpitations, and weight loss.

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