Literature DB >> 27574996

Hypercalcemia in Patients with Williams-Beuren Syndrome.

Sampat Sindhar1, Michael Lugo1, Mark D Levin2, Joshua R Danback1, Benjamin D Brink3, Eric Yu3, Dennis J Dietzen1, Amy L Clark1, Carolyn A Purgert1, Jessica L Waxler4, Robert W Elder5, Barbara R Pober6, Beth A Kozel7.   

Abstract

OBJECTIVE: To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study. STUDY
DESIGN: Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities.
RESULTS: On average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported.
CONCLUSIONS: Actionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis. Published by Elsevier Inc.

Entities:  

Keywords:  calcium; not in the title: QTc; pediatric reference intervals

Mesh:

Substances:

Year:  2016        PMID: 27574996      PMCID: PMC5085847          DOI: 10.1016/j.jpeds.2016.08.027

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  31 in total

1.  The Williams elfin facies syndrome. A new perspective.

Authors:  K L Jones; D W Smith
Journal:  J Pediatr       Date:  1975-05       Impact factor: 4.406

Review 2.  Hypercalcemia in children and adolescents.

Authors:  Steven A Lietman; Emily L Germain-Lee; Michael A Levine
Journal:  Curr Opin Pediatr       Date:  2010-08       Impact factor: 2.856

3.  Rickets in an infant with Williams syndrome.

Authors:  R S Mathias
Journal:  Pediatr Nephrol       Date:  2000-06       Impact factor: 3.714

4.  Adults with Williams syndrome.

Authors:  C A Morris; C O Leonard; C Dilts; S A Demsey
Journal:  Am J Med Genet Suppl       Date:  1990

5.  Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome.

Authors:  Cinzia Sforzini; Donatella Milani; Emilio Fossali; Anna Barbato; Gianpaolo Grumieri; Mario G Bianchetti; Angelo Selicorni
Journal:  Pediatr Nephrol       Date:  2002-10-09       Impact factor: 3.714

6.  Symptomatic hypercalcemia in the first months of life: calcium-regulating hormones and treatment.

Authors:  P Ghirri; U Bottone; L Coccoli; M Bernardini; M Vuerich; A Cuttano; C Riparbelli; G Pellegrinetti; A Boldrini
Journal:  J Endocrinol Invest       Date:  1999-05       Impact factor: 4.256

Review 7.  FISH analysis in patients with clinical diagnosis of Williams syndrome.

Authors:  N Elçioglu; C Mackie-Ogilvie; M Daker; A C Berry
Journal:  Acta Paediatr       Date:  1998-01       Impact factor: 2.299

8.  Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients.

Authors:  C A Joyce; B Zorich; S J Pike; J C Barber; N R Dennis
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

Review 9.  Importance of dietary calcium and vitamin D in the treatment of hypercalcaemia in Williams-Beuren syndrome.

Authors:  Anke L L Lameris; Christel L M Geesing; Joost G J Hoenderop; Michiel F Schreuder
Journal:  J Pediatr Endocrinol Metab       Date:  2014-07       Impact factor: 1.634

10.  Severe hypercalcemia without hypercalciuria in a previously healthy infant.

Authors:  Bradley C Clark; Rita Fleming; Michael C Spaeder; Shamir Tuchman
Journal:  J Pediatr Endocrinol Metab       Date:  2012       Impact factor: 1.634

View more
  9 in total

1.  Glucose and lipid metabolism, bone density, and body composition in individuals with Williams syndrome.

Authors:  Sofia Shaikh; Jessica L Waxler; Hang Lee; Kathy Grinke; Jamie Garry; Barbara R Pober; Takara L Stanley
Journal:  Clin Endocrinol (Oxf)       Date:  2018-09-18       Impact factor: 3.478

Review 2.  Hypercalcemia: a consultant's approach.

Authors:  Ari Auron; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2017-09-06       Impact factor: 3.714

3.  Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.

Authors:  Michael Lugo; Zoë C Wong; Charles J Billington; Phoebe C R Parrish; Glennis Muldoon; Delong Liu; Barbara R Pober; Beth A Kozel
Journal:  Am J Med Genet A       Date:  2020-02-20       Impact factor: 2.578

4.  Williams-Beuren syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Deise Helena de Souza; Angélica Moresco; Victoria Huckstadt; Ashleigh D Gill; Alec P Boyle; Tommy Hu; Yonit A Addissie; Gary T K Mok; Cedrik Tekendo-Ngongang; Karen Fieggen; Eloise J Prijoles; Pranoot Tanpaiboon; Engela Honey; Ho-Ming Luk; Ivan F M Lo; Meow-Keong Thong; Premala Muthukumarasamy; Kelly L Jones; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Laila Bouguenouch; Anju Shukla; Katta M Girisha; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Monisha S Kisling; Carlos R Ferreira; María Beatriz de Herreros; Ni-Chung Lee; Saumya S Jamuar; Angeline Lai; Ee Shien Tan; Jiin Ying Lim; Cham Breana Wen-Min; Neerja Gupta; Stephanie Lotz-Esquivel; Ramsés Badilla-Porras; Dalia Farouk Hussen; Mona O El Ruby; Engy A Ashaat; Siddaramappa J Patil; Leah Dowsett; Alison Eaton; A Micheil Innes; Vorasuk Shotelersuk; Ëben Badoe; Ambroise Wonkam; María Gabriela Obregon; Brian H Y Chung; Milana Trubnykova; Jorge La Serna; Bertha Elena Gallardo Jugo; Miguel Chávez Pastor; Hugo Hernán Abarca Barriga; Andre Megarbane; Beth A Kozel; Mieke M van Haelst; Roger E Stevenson; Marshall Summar; A Adebowale Adeyemo; Colleen A Morris; Danilo Moretti-Ferreira; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.578

5.  Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.

Authors:  Yu Xia; Shufang Huang; Yueheng Wu; Yongchao Yang; Shaoxian Chen; Ping Li; Jian Zhuang
Journal:  Mol Genet Genomic Med       Date:  2018-12-18       Impact factor: 2.183

6.  A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells.

Authors:  Rossella De Cegli; Simona Iacobacci; Anthony Fedele; Andrea Ballabio; Diego di Bernardo
Journal:  Sci Data       Date:  2019-11-06       Impact factor: 6.444

Review 7.  Nephrocalcinosis: A Review of Monogenic Causes and Insights They Provide into This Heterogeneous Condition.

Authors:  Fay J Dickson; John A Sayer
Journal:  Int J Mol Sci       Date:  2020-01-06       Impact factor: 5.923

Review 8.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

Review 9.  Genetic causes of neonatal and infantile hypercalcaemia.

Authors:  Caroline M Gorvin
Journal:  Pediatr Nephrol       Date:  2021-05-14       Impact factor: 3.714

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.