Cargando…

Immobilization-induced hypercalcemia in a patient with renal failure

SUMMARY: Immobilization-induced hypercalcemia is an uncommon cause of elevated calcium which is usually diagnosed following extensive systemic workup and exclusion of more common etiologies. Previously reported cases have largely described this phenomenon in adolescents and young adults a few weeks...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gandhi, Anand, Mortensen, Mike, Sunny, Sonie, Techathaveewat, Pawarid, Targovnik, Jerome, Alsayed, Mahmoud
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2021
Materias:	New Disease or Syndrome: Presentations/Diagnosis/Management
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558878/ https://www.ncbi.nlm.nih.gov/pubmed/34612208 http://dx.doi.org/10.1530/EDM-21-0086

Ejemplares similares

A rare case of ectopic ACTH syndrome caused by primary renal neuroendocrine tumor
por: Chunharojrith, Paweena, et al.
Publicado: (2021)

Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities
por: Du, Yang Timothy, et al.
Publicado: (2019)

Familial partial lipodystrophy and proteinuric renal disease due to a missense c.1045C > T LMNA mutation
por: Fountas, Athanasios, et al.
Publicado: (2017)

Histologically confirmed isolated IgG4-related hypophysitis: two case reports in young women
por: Sosa, Gabriela Alejandra, et al.
Publicado: (2014)

Ectopic prolactin secretion secondary to an ovarian tumour
por: Gururaj, Sowmya, et al.
Publicado: (2013)

Ovarian cyst regression with levothyroxine in ovarian hyperstimulation syndrome associated with hypothyroidism
por: Langroudi, Roghieh Molaei, et al.
Publicado: (2013)

Steroid cell tumor: a rare cause of hirsutism in a female
por: Swain, Jayshree, et al.
Publicado: (2013)

Multiple Hürthle cell adenomas in a patient with thyroid hormone resistance
por: Xifra, Gemma, et al.
Publicado: (2013)

Parasitic thyroid nodules: cancer or not?
por: Baker, Lauren J, et al.
Publicado: (2014)

Pituitary injury and persistent hypofunction resulting from a peripartum non-hemorrhagic, vaso-occlusive event
por: Kuriya, Anita, et al.
Publicado: (2015)

The importance of IgG4 in the predictive model of thyroiditis
por: Pandrc, Milena S, et al.
Publicado: (2015)

Thyroid lipomatosis in a 36-year-old patient with rheumatoid arthritis and a kidney transplant
por: Bell, Soledad, et al.
Publicado: (2016)

A Greek girl with 11β-hydroxylase deficiency due to compound heterozygosity for two novel mutations in CYP11B1 gene
por: Marakaki, Chrisanthi, et al.
Publicado: (2015)

Fatal outcome in a Hispanic woman with moyamoya syndrome and Graves’ disease
por: Choi, Julian, et al.
Publicado: (2016)

Cytomegalovirus-mononucleosis-induced thyroiditis in an immunocompetent patient
por: Larouche, V, et al.
Publicado: (2017)

A patient with a germline SDHB mutation presenting with an isolated pituitary macroprolactinoma
por: Maher, Michelle, et al.
Publicado: (2018)

Achondroplasia with SRY-positive 46, XX disorder of sex development: an extremely rare association
por: Du, Yang Timothy, et al.
Publicado: (2018)

Prolonged diabetic ketoacidosis associated with canagliflozin
por: Sloan, Gordon, et al.
Publicado: (2018)

Persistent impairment in working memory following severe hyperglycemia in newly diagnosed type 2 diabetes
por: Cerasuolo, Joseph, et al.
Publicado: (2017)

Primary high-grade calcitonin-negative neuroendocrine carcinoma of the thyroid: a very rare cancer
por: Chorny, Joseph A, et al.
Publicado: (2018)

DICER1 mutation and pituitary prolactinoma
por: Cotton, Ellena, et al.
Publicado: (2018)

A novel CASR mutation (p.Glu757Lys) causing autosomal dominant hypocalcaemia type 1
por: Kwan, Benjamin, et al.
Publicado: (2018)

A clinically functioning gonadotroph adenoma presenting with abdominal pain, ovarian hyperstimulation and fibromatosis
por: Broughton, Chloe, et al.
Publicado: (2018)

Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1
por: Jhawar, Sakshi, et al.
Publicado: (2019)

Concurrent intrathyroidal thymus and parathyroid in a patient with papillary thyroid carcinoma: a challenging diagnosis
por: Velimezis, Georgios, et al.
Publicado: (2017)

Novel germline variant of TMEM127 gene in a patient with familial pheochromocytoma
por: Saitoh, Kohei, et al.
Publicado: (2017)

Euthyroid athyroxinemia – a novel endocrine syndrome
por: Woodhouse, Nicholas, et al.
Publicado: (2017)

A novel stop mutation (p.(Gln22*)) of DAX1 (NR0B1) results in late-onset X-linked adrenal hypoplasia congenita
por: Gerards, Judith, et al.
Publicado: (2017)

A rare cause of metabolic acidosis: ketoacidosis in a non-diabetic lactating woman
por: Sloan, Gordon, et al.
Publicado: (2017)

An autoimmune cause of confusion in a patient with a background of hypothyroidism
por: Brown, Jonathan, et al.
Publicado: (2019)

First-positive surveillance screening in an asymptomatic SDHA germline mutation carrier
por: White, Gemma, et al.
Publicado: (2019)

Insulin autoimmune syndrome
por: Yukina, Marina, et al.
Publicado: (2020)

A novel CASR variant in a family with familial hypocalciuric hypercalcaemia and primary hyperparathyroidism
por: Sagi, Satyanarayana V, et al.
Publicado: (2020)

Metastatic insulinoma presenting 14 years after benign tumour resection: a rare case and management dilemma
por: Keen, F, et al.
Publicado: (2020)

Coexistence of DIPNECH and carotid body paraganglioma: is it just a coincidence?
por: Pedro, J, et al.
Publicado: (2020)

A novel TRPM6 variant (c.3179T>A) causing familial hypomagnesemia with secondary hypocalcemia
por: Lomelino-Pinheiro, Sara, et al.
Publicado: (2020)

Type B insulin resistance syndrome associated with connective tissue disease and psoriasis
por: Łebkowska, Agnieszka, et al.
Publicado: (2020)

Concomitant medullary thyroid carcinoma with paraganglioma-like pattern and papillary thyroid carcinoma
por: Greco, C, et al.
Publicado: (2019)

A sarcoidosis–lymphoma syndrome revealed by hypopituitarism
por: Delcourt, Charlotte, et al.
Publicado: (2019)

Methotrexate-associated lymphoproliferative disorder with hypopituitarism and central diabetes insipidus
por: Aoshima, Misaki, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_ba7ein10l0cut93vop7e55sg2k