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Calcitriol in the Treatment of Osteoporosis Post-Menopause

Case Study:  Patient Profile: Name: Helen Martinez (hypothetical) Age: 58 years Medical History: Post-menopausal, recently diagnosed with osteoporosis, history of minor fractures, and vitamin D.

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Implications for Acromegaly and Neuroendocrine Tumors

Unraveling the GIP-Somatostatin Tango: Acromegaly, a debilitating condition characterized by excessive growth hormone (GH) secretion, and neuroendocrine tumors (NETs), a heterogenous group of neoplasms arising.

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Deciphering the Incretin Dance in Prader-Willi Syndrome

GIP vs. GLP-1: Abstract: Prader-Willi syndrome (PWS) is a complex genetic disorder characterized by insatiable hunger, hyperphagia, and dysregulation of multiple metabolic pathways. Incretins, gut-derived.

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Sarah and the GLP-1 vs. GIP Tango

Case Study:  Sarah, a 15-year-old girl with PWS, struggles with constant hunger and weight management. Despite following a strict diet and exercise program, she grapples.

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Melody’s Journey Through the Hormonal Maze

Case Study:  Melody, a bubbly 28-year-old artist, dreamt of creating a family art project – her children. Yet, PCOS and whispers of “prolactin imbalance” threw.

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Fueling the Giant Growth Show

Glucagon’s Encore in Acromegaly:  Acromegaly, a hormonal disorder characterized by excessive growth hormone (GH) production, has long captivated medical science with its dramatic manifestations. The.

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: Conducting Chaos in Graves’ Disease

Glucagon and the Thyroid Orchestra Imagine a symphony gone rogue, instruments blaring off-key, tempos erratic, and the conductor lost in a feverish frenzy. This is.

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Taming the Sugar Blues in Type 2.

Case Study:  The intertwined relationship between stress, blood sugar, and emotional well-being in type 2 diabetes is a complex and under-recognized challenge. This case study.

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A Case Study of Loss and Love.

Cradle Robbed:  Maryam, a 32-year-old woman with eyes bright as hope and a smile etched with exhaustion, sat cradling her newborn son, Ali. The delivery,.

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The Silent Tango

Case Study: Patient: 23-year-old male with delayed puberty and absent sense of smell. Diagnosis: Kallmann syndrome, confirmed by genetic testing. Challenges: Low LH and FSH.

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