Literature DB >> 22293055

Rickets in Denmark.

Signe Sparre Beck-Nielsen1.   

Abstract

Rickets is a heterogeneous group of diseases of the growing child caused by defect mineralization of bone. Nutritional rickets is caused by deficiency of vitamin D, calcium or both. Several hereditary forms of rickets exist where the disease proceeds into adulthood. Nutritional rickets was common in the past, but by introduction of preventative administration of cod liver oil and vitamin D supplementation, nutritional rickets became a rarity. During the last decades, case reports of nutritional rickets reappear in the industrialized countries. It is the general conception that in the industrialized countries, hereditary rickets is the most prevalent cause of rickets today. However, the incidence of nutritional rickets and the incidence and prevalence of hereditary rickets in Scandinavia are unknown. The most common form of hereditary rickets is hypophosphatemic rickets (HR). The geno- and phenotype among Scandinavian patients have not been characterized. Especially, the disease in adult patients is not well described. Moreover, there are conflicting reports of the benefits of medical treatment throughout childhood, and in addition on gender differences in disease severity.

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Year:  2012        PMID: 22293055

Source DB:  PubMed          Journal:  Dan Med J        ISSN: 2245-1919            Impact factor:   1.240


  3 in total

1.  Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemia.

Authors:  Hans Gjørup; Signe Sparre Beck-Nielsen; Dorte Haubek
Journal:  Clin Oral Investig       Date:  2017-06-12       Impact factor: 3.573

Review 2.  "English Disease": Historical Notes on Rickets, the Bone-Lung Link and Child Neglect Issues.

Authors:  Mingyong Zhang; Fan Shen; Anna Petryk; Jingfeng Tang; Xingzhen Chen; Consolato Sergi
Journal:  Nutrients       Date:  2016-11-15       Impact factor: 5.717

Review 3.  FGF23 and its role in X-linked hypophosphatemia-related morbidity.

Authors:  Signe Sparre Beck-Nielsen; Zulf Mughal; Dieter Haffner; Ola Nilsson; Elena Levtchenko; Gema Ariceta; Carmen de Lucas Collantes; Dirk Schnabel; Ravi Jandhyala; Outi Mäkitie
Journal:  Orphanet J Rare Dis       Date:  2019-02-26       Impact factor: 4.123

  3 in total

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