Hypophosphatasia in adolescents and adults: overview of diagnosis and treatment

被引:0
作者
M. L. Bianchi
N. J. Bishop
N. Guañabens
C. Hofmann
F. Jakob
C. Roux
M. C. Zillikens
机构
[1] Istituto Auxologico Italiano IRCCS,Laboratorio sperimentale di ricerche sul metabolismo osseo infantile, Centro Malattie Metaboliche Ossee
[2] University of Sheffield,Department of Oncology and Metabolism
[3] Sheffield Children’s NHS Foundation Trust,Servicio de Reumatología, Hospital Clínic
[4] Universidad de Barcelona,Children’s Hospital
[5] IDIBAPS CIBERehd,Orthopedic Centre for Musculoskeletal Research
[6] University of Würzburg,INSERM U1153 APHP Centre
[7] University of Würzburg,Department of Internal Medicine
[8] Université de Paris,undefined
[9] Department of Rheumatology,undefined
[10] Endocrinology Section,undefined
[11] Erasmus Medical Centre,undefined
来源
Osteoporosis International | 2020年 / 31卷
关键词
Alkaline phosphatase; Bone; Fractures; Hypomineralization; Hypophosphatasia; Teeth;
D O I
暂无
中图分类号
学科分类号
摘要
This article provides an overview of the current knowledge on hypophosphatasia—a rare genetic disease of very variable presentation and severity—with a special focus on adolescents and adults. It summarizes the available information on the many known mutations of tissue-nonspecific alkaline phosphatase (TNSALP), the epidemiology and clinical presentation of the disease in adolescents and adults, and the essential diagnostic clues. The last section reviews the therapeutic approaches, including recent reports on enzyme replacement therapy (EnzRT).
引用
收藏
页码:1445 / 1460
页数:15
相关论文
共 50 条
  • [31] Possible role of bone turnover markers in the diagnosis of adult hypophosphatasia
    Bertoldo, Francesco
    Tripepi, Giovanni
    Zaninotto, Martina
    Plebani, Mario
    Scillitani, Alfredo
    Varenna, Massimo
    Crotti, Chiara
    Cipriani, Cristiana
    Pepe, Jessica
    Minisola, Salvatore
    Pugliese, Flavia
    Guarnieri, Vito
    Baffa, Valeria
    Torres, Marco Onofrio
    Zanchetta, Francesca
    Fusaro, Maria
    Rossini, Maurizio
    Brandi, Maria Luisa
    Egan, Colin Gerard
    Simioni, Paolo
    Arcidiacono, Gaetano Paride
    Sella, Stefania
    Giannini, Sandro
    JOURNAL OF BONE AND MINERAL RESEARCH, 2024, 40 (01) : 79 - 86
  • [32] Hypophosphatasia: Review of Bone Mineral Metabolism, Pathophysiology, Clinical Presentation, Diagnosis, and Treatment
    Meah F.
    Basit A.
    Emanuele N.
    Emanuele M.A.
    Clinical Reviews in Bone and Mineral Metabolism, 2017, 15 (1): : 24 - 36
  • [33] Pediatric hypophosphatasia: avoid diagnosis missteps!
    Whyte, Michael P.
    McAlister, William H.
    Mack, Karen E.
    Mumm, Steven
    Madson, Katherine L.
    JOURNAL OF BONE AND MINERAL RESEARCH, 2024, 39 (06) : 655 - 660
  • [34] Active search of adult patients with persistently low serum alkaline phosphatase levels for the diagnosis of hypophosphatasia
    Rocha Vieira, Lucio Henrique
    Peixoto, Kleison Cordeiro
    Flosi, Caroline Leal
    Fleiuss de Farias, Maria Lucia
    Madeira, Miguel
    ARCHIVES OF ENDOCRINOLOGY METABOLISM, 2021, 65 (03): : 289 - 294
  • [35] The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance
    Maria Luisa Brandi
    Aliya A. Khan
    Eric T. Rush
    Dalal S. Ali
    Hatim Al-Alwani
    Khulod Almonaei
    Farah Alsarraf
    Severine Bacrot
    Kathryn M. Dahir
    Karel Dandurand
    Chad Deal
    Serge Livio Ferrari
    Francesca Giusti
    Gordon Guyatt
    Erin Hatcher
    Steven W. Ing
    Muhammad Kassim Javaid
    Sarah Khan
    Roland Kocijan
    E. Michael Lewiecki
    Agnes Linglart
    Iman M’Hiri
    Francesca Marini
    Mark E. Nunes
    Cheryl Rockman-Greenberg
    Lothar Seefried
    Jill H. Simmons
    Susan R. Starling
    Leanne M. Ward
    Liang Yao
    Romina Brignardello-Petersen
    Christian Roux
    Osteoporosis International, 2024, 35 : 439 - 449
  • [36] The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance
    Brandi, Maria Luisa
    Khan, Aliya A.
    Rush, Eric T.
    Ali, Dalal S.
    Al-Alwani, Hatim
    Almonaei, Khulod
    Alsarraf, Farah
    Bacrot, Severine
    Dahir, Kathryn M.
    Dandurand, Karel
    Deal, Chad
    Ferrari, Serge Livio
    Giusti, Francesca
    Guyatt, Gordon
    Hatcher, Erin
    Ing, Steven W.
    Javaid, Muhammad Kassim
    Khan, Sarah
    Kocijan, Roland
    Lewiecki, E. Michael
    Linglart, Agnes
    M'Hiri, Iman
    Marini, Francesca
    Nunes, Mark E.
    Rockman-Greenberg, Cheryl
    Seefried, Lothar
    Simmons, Jill H.
    Starling, Susan R.
    Ward, Leanne M.
    Yao, Liang
    Brignardello-Petersen, Romina
    Roux, Christian
    OSTEOPOROSIS INTERNATIONAL, 2024, 35 (03) : 431 - 438
  • [37] Clinical and Genetic Characteristics of Hypophosphatasia in Chinese Adults
    Li, Xiang
    Ren, Na
    Wang, Ziyuan
    Wang, Ya
    Hu, Yunqiu
    Hu, Weiwei
    Gu, Jiemei
    Hong, Wei
    Zhang, Zhenlin
    Wang, Chun
    GENES, 2023, 14 (04)
  • [38] Clinical and biochemical characteristics of adults with hypophosphatasia attending a metabolic bone clinic
    Desborough, Robert
    Nicklin, Philip
    Gossiel, Fatma
    Balasubramanian, Meena
    Walsh, Jennifer S.
    Petryk, Anna
    Teynor, Megan
    Eastell, Richard
    BONE, 2021, 144
  • [39] Urine phosphoethanolamine is a specific biomarker for hypophosphatasia in adults
    Shajani-Yi, Zahra
    Ayala-Lopez, Nadia
    Black, Margo
    Dahir, Kathryn McCrystal
    BONE, 2022, 163
  • [40] Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives
    Amaka C. Offiah
    Jerry Vockley
    Craig F. Munns
    Jun Murotsuki
    Pediatric Radiology, 2019, 49 : 3 - 22