Results 81 to 90 of about 1,412 (173)
A case of normocalcemic primary hyperparathyroidism with osteomalacia.
A 59 year-old patient had lumbago and pain in hip joints, knees, and ribs of long duration. Severe hypophosphatemia and high serum ionized calcium were found in spite of normal level of total serum calcium. The serum parathyroid hormone and alkaline phosphatase levels were elevated, and diffuse demineralization of the bones and renal stones were found ...
SHIMADA, ICHIRO +5 more
openaire +3 more sources
World Journal of Surgery, Volume 49, Issue 1, Page 115-116, January 2025.
Christine J. O’Neill
wiley +1 more source
Epidemiology and Clinical Forms of Primary Hyperparathyroidism: A Review
Primary hyperparathyroidism (PHPT) is a disease caused by overactive parathyroid glands with consequent hypercalcemia. However, its presentation is variable, with patients demonstrating a range from normocalcemia to severe hypercalcemic PHPT. The present
Oliveira, Paula Aragão P. de +6 more
core +1 more source
[Normocalcemic primary hyperparathyroidism].
This report shows our conclusions on the clinical, biochemical and densitometry characteristics of 35 normocalcemic primary hyperparathyroidism (PHPT) patients. This condition is defined by a high level of intact parathyroid hormone (iPTHI) with persistently normal serum and ionized calcium in the absence of secondary hyperparathyroidism. Our selection
Francisco R, Spivacow +2 more
openaire +1 more source
Normocalcemic primary hyperparathyroidism (NC-PHPT) is a variant of hyperparathyroidism, characterized by normal serum calcium levels, high parathyroid hormone (PTH) and normal 25-OH vitamin D status.
Caliskan, Mustafa +6 more
core +2 more sources
Objective . To report a case of severe hypercalcemia, exacerbated by vitamin A supplementation and hydrochlorothiazide, in a patient with primary hyperparathyroidism. Methods . Clinical and laboratory findings are presented along with response to therapy.
Ron T. Varghese MBBS +5 more
doaj +1 more source
Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene.
BACKGROUND: Familial isolated primary hyperparathyroidism (FIHP) is an autosomal dominant disorder that can represent an early stage of either the multiple endocrine neoplasia type 1 (MEN1) or hyperparathyroidism-jaw tumor (HPT-JT) syndromes ...
Fadil M Hannan +15 more
core +1 more source
Identification and characterization of normocalcemic primary hyperparathyroidism in Health Areas I and II of the Community of Cantabria [PDF]
RESUMEN: El hiperparatiroidismo primario normocalcémico es una entidad aún poco conocida. Este estudio pretende caracterizar los casos de hiperparatiroidismo primario normocalcémico detectados durante un año completo en las áreas I y II de salud de ...
Santana Hernández, Borja
core
OBJECTIVE: To describe the characteristics of normocalcemic primary hyperparathyroidism (NPHPT) in patients seen for osteoporosis evaluation. PATIENTS AND METHODS: We examined the records of 156 women who came to the hospital to be screened for ...
Francisco Bandeira +5 more
core +1 more source
Incidental Normocalcemic Primary Hyperparathyroidism Presenting With Symptomatic Hypophosphatemia: A Case Report. [PDF]
Tabbikha O, Chamy J, El Khoury M.
europepmc +1 more source

