Familial hypocalciuric hypercalcemia. About two cases

被引：0
|
作者：
Gonzalez-Gonzalez, A. [1 ]
Del Rey, M. Delgado [1 ]
Dominguez-Osorio, I [2 ]
Cordova, J. M. Recio [3 ]
机构：
[1] Hosp Gen Univ Ciudad Real, Secc Endocrinol & Nutr, Ciudad Real, Spain
[2] HGUCR Hosp Gen Univ Ciudad Real, Serv Med Interna, Ciudad Real, Spain
[3] Complejo Asistencial Univ Salamanca, Serv Endocrinol & Nutr, Salamanca, Spain
来源：
REVISTA DE OSTEOPOROSIS Y METABOLISMO MINERAL | 2022年 / 14卷 / 02期
关键词：
PRIMARY HYPERPARATHYROIDISM;
D O I：
10.4321/S1889-836X2022000200001
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：67 / 68
页数：2
相关论文
共 50 条
  • [31] A novel mutation of the calcium-sensing receptor gene in a German subject with familial hypocalciuric hypercalcemia and primary hyperparathyroidism
    Papadakis, Marios
    Meurer, Natalie
    Margariti, Theodora
    Meyer, Anke
    Weyerbrock, Norbert
    Dotzenrath, Cornelia
    HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2016, 15 (04): : 557 - 559
  • [32] Efficacy of calcium excretion and calcium/creatinine clearance ratio in the differential diagnosis of familial hypocalciuric hypercalcemia and primary hyperparathyroidism
    Bhangu, Jagdeep Singh
    Selberherr, Andreas
    Brammen, Lindsay
    Scheuba, Christian
    Riss, Philipp
    HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2019, 41 (05): : 1372 - 1378
  • [33] A novel mutation of the calcium-sensing receptor gene in a German subject with familial hypocalciuric hypercalcemia and primary hyperparathyroidism
    Marios Papadakis
    Natalie Meurer
    Theodora Margariti
    Anke Meyer
    Norbert Weyerbrock
    Cornelia Dotzenrath
    Hormones, 2016, 15 : 557 - 559
  • [34] AP2S1 and GNA11 mutations - not a common cause of familial hypocalciuric hypercalcemia
    Hovden, Silje
    Rejnmark, Lars
    Ladefoged, Soren A.
    Nissen, Peter H.
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2017, 176 (02) : 177 - 185
  • [35] Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population
    Dershem, Ridge
    Gorvin, Caroline M.
    Metpally, Raghu P. R.
    Krishnamurthy, Sarathbabu
    Smelser, Diane T.
    Hannan, Fadil M.
    Carey, David J.
    Thakker, Rajesh, V
    Breitwieser, Gerda E.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2020, 106 (06) : 734 - 747
  • [36] Clinical and outcome comparison of genetically positive vs. negative patients in a large cohort of suspected familial hypocalciuric hypercalcemia
    Asla, Queralt
    Sarda, Helena
    Segui, Nuria
    Martinez de Pinillos, Guillermo
    Mazarico-Altisent, Isabel
    Capel, Ismael
    Rives, Jose
    Suarez, Javier
    avila-Rubio, Veronica
    Munoz Torres, Manuel
    Saigi, Ignasi
    Palacios, Nuria
    Urgell, Eulalia
    Webb, Susan M.
    Fernandez, Merce
    Oriola, Josep
    Mora, Mireia
    Tondo, Mireia
    Aulinas, Anna
    ENDOCRINE, 2024, 83 (03) : 747 - 756
  • [37] Multiple endocrine neoplasia phenocopy revealed as a co-occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
    Hovden, Silje
    Jespersen, Marie Louise
    Nissen, Peter H.
    Poulsen, Per Logstrup
    Rolighed, Lars
    Ladefoged, Soren A.
    Rejnmark, Lars
    CLINICAL CASE REPORTS, 2016, 4 (10): : 922 - 927
  • [38] A novel mutation in the calcium-sensing receptor gene in an Irish pedigree showing familial hypocalciuric hypercalcemia: a case report
    Wael F Elamin
    Olivier de Buyl
    Journal of Medical Case Reports, 4 (1)
  • [39] Increased Trabecular Volumetric Bone Mass Density in Familial Hypocalciuric Hypercalcemia (FHH) Type 1: A Cross-Sectional Study
    Jakobsen, Niels Frederik Breum
    Rolighed, Lars
    Moser, Emil
    Nissen, Peter H.
    Mosekilde, Leif
    Rejnmark, Lars
    CALCIFIED TISSUE INTERNATIONAL, 2014, 95 (02) : 141 - 152
  • [40] Misleading localization by 18F-fluorocholine PET/CT in familial hypocalciuric hypercalcemia type-3: a case report
    Mukhtar, Noha N.
    Abouzied, Mohei El-Din M.
    Alqahtani, Mohammed H.
    Hammami, Muhammad M.
    BMC ENDOCRINE DISORDERS, 2021, 21 (01)
12345