The prevalence of familial hypocalciuric hypercalcemia

被引:47
作者
Hinnie, J [1 ]
Bell, E
McKillop, E
Gallacher, S
机构
[1] Paisley Royal Alexandra Hosp, Med Directorate, Dept Med, Paisley PA2 9PN, Renfrew, Scotland
[2] Glasgow Royal Infirm, Dept Biochem, Glasgow G4 0SF, Lanark, Scotland
[3] Univ Glasgow, Glasgow Royal Infirm, Dept Med, Glasgow G4 0SF, Lanark, Scotland
[4] So Gen Hosp, Med Unit, Glasgow G51 4TF, Lanark, Scotland
关键词
familial hypocalciuric hypercalcemia; familial benign hypercalcemia; hypercalcamia; hyperparathyroidism;
D O I
10.1007/s002230001201
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Familial hypocalciuric hypercalcamia is said to be an extremely rare condition but is clinically important because it can be confused with primary hyperparathyroidism. The biochemical features of the two conditions are similar, but the former is benign while the latter can have serious clinical consequences with patients occasionally proceeding to parathyroidectomy. It is therefore important to differentiate accurately between the two. With this in mind it would be useful to know the prevalence of familial hypocalciuric hypercalcemia when considering the differential diagnosis of primary hyperparathyroidism. However. as far as we are aware, no estimate of the prevalence of this condition can be found in the literature. We describe how an estimate was made of the prevalence of familial hypocalciuric hypercalcemia in the west of Scotland. We estimate the prevalence to be 1 in 78,000 at least.
引用
收藏
页码:216 / 218
页数:3
相关论文
共 50 条
  • [21] Identification and functional analysis of a novel CaSR mutation in a family with familial hypocalciuric hypercalcemia
    Kim, Eun Sook
    Kim, Su Yeon
    Lee, Ji Young
    Han, Je Ho
    Sohn, Tae Seo
    Son, Hyun Shik
    Moon, Sung-dae
    JOURNAL OF BONE AND MINERAL METABOLISM, 2016, 34 (06) : 662 - 667
  • [22] Kabuki Syndrome and Crohn Disease in a Child with Familial Hypocalciuric Hypercalcemia
    Ho, Josephine
    Fox, Danya
    Innes, A. Micheil
    McLeod, Ross
    Butzner, Decker
    Johnson, Nicole
    Trevenen, Cynthia
    Kendrick, Victoria
    Cole, David E. C.
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2010, 23 (09) : 975 - 979
  • [23] Spontaneous rib fractures in a black woman with familial hypocalciuric hypercalcemia
    Mohammed, Reerna
    Bray, Marilyn B.
    Koch, Christian A.
    Uwaifo, Gabriel I.
    MEDICAL SCIENCE MONITOR, 2008, 14 (10): : CS102 - CS106
  • [24] Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature review
    Zahedi, Maryam
    Arani, Reyhane Hizomi
    Rafati, Maryam
    Amouzegar, Atieh
    Hadaegh, Farzad
    BMC ENDOCRINE DISORDERS, 2021, 21 (01)
  • [25] Calcium metabolism and endocrine functions in a family with familial hypocalciuric hypercalcemia
    Speer, G
    Tóth, M
    Niller, HH
    Salamon, D
    Takács, I
    Miheller, P
    Patócs, A
    Nagy, Z
    Bajnok, É
    Nyiri, P
    Lakatos, P
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2003, 111 (08) : 486 - 490
  • [26] Singular case report of familial hypocalciuric hypercalcemia: a rare diagnosis of hypercalcemia in the older people
    Ojardias, Etienne
    Leman, Melanie
    Lafaie, Ludovic
    Oriol, Philippe
    Calmels, Paul
    Celarier, Thomas
    AGING MALE, 2025, 28 (01)
  • [27] Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature review
    Maryam Zahedi
    Reyhane Hizomi Arani
    Maryam Rafati
    Atieh Amouzegar
    Farzad Hadaegh
    BMC Endocrine Disorders, 21
  • [28] Diffuse Idiopathic Skeletal Hyperostosis and Familial Hypocalciuric Hypercalcemia: A Unique Association in a Young Female
    Rivas, Ana M.
    Lado-Abeal, Joaquin
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2013, 346 (03) : 247 - 249
  • [29] Familial hypocalciuric hypercalcemia: new mutation in the CASR gene converting valine 697 to methionine
    Aparicio Lopez, Cristina
    Anton-Martin, Pilar
    Gil-Fournier, Belen
    Ramiro-Leon, Soraya
    Perez-Nanclares, Gustavo
    Perez de Nanclares, Guiomar
    Martinez Menendez, Beatriz
    Castano, Luis
    EUROPEAN JOURNAL OF PEDIATRICS, 2012, 171 (01) : 147 - 150
  • [30] Familial hypocalciuric hypercalcemia caused by homozygousCaSRgene mutation A case report of a family
    Wang, Feifei
    Hu, Jia
    Mei, Chao
    Lin, Xia
    Zhang, Ling
    MEDICINE, 2020, 99 (35) : E21940