Pituitary function studies are essential diagnostic tools used to assess the secretory capacity of the anterior and posterior pituitary gland, helping clinicians diagnose, manage, and…
Pituitary dwarfism, also referred to as growth hormone deficiency (GHD), is a rare condition that results in abnormally short stature due to insufficient production of…
Pinta is a chronic, non-venereal infectious skin disease caused by Treponema carateum, a bacterium closely related to the causative agent of syphilis. This condition is…
PIK3CA-related overgrowth spectrum (PROS) comprises a group of rare disorders characterized by somatic mutations in the PIK3CA gene, leading to abnormal tissue growth in multiple…
Philadelphia chromosome-positive chronic myelocytic leukemia (Ph+ CML) is a hematopoietic stem cell disorder characterized by unregulated myeloid cell proliferation, resulting from the formation of the…
Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) represents a high-risk subtype of ALL, characterized by the presence of the BCR-ABL1 fusion gene resulting from a…
Pheochromocytoma Adjunct Therapy: Pheochromocytoma is a catecholamine-secreting tumor that primarily arises from the adrenal medulla. While surgical resection remains the cornerstone of treatment, adjunct therapies…
Pheochromocytoma is a rare catecholamine-producing tumor that arises from the chromaffin cells of the adrenal medulla. It is characterized by excessive secretion of epinephrine, norepinephrine,…
Phenylketonuria (PKU) is a rare but serious autosomal recessive metabolic disorder that affects the body's ability to metabolize the amino acid phenylalanine. Without prompt diagnosis…
Pharyngitis Due to Streptococcus pyogenes: Pharyngitis caused by Streptococcus pyogenes, also known as Group A Streptococcus (GAS), represents one of the most common and clinically…