Demographic Characteristics, Risk Factors, and Presenting Features of Children with Symptomatic Nutritional Rickets: A French Series.


Journal

Hormone research in paediatrics
ISSN: 1663-2826
Titre abrégé: Horm Res Paediatr
Pays: Switzerland
ID NLM: 101525157

Informations de publication

Date de publication:
2020
Historique:
received: 26 05 2020
accepted: 03 09 2020
pubmed: 30 10 2020
medline: 6 10 2021
entrez: 29 10 2020
Statut: ppublish

Résumé

To describe the demographic characteristics, risk factors, and presenting features of children with symptomatic nutritional rickets in France. This is a retrospective study of 38 children diagnosed with nutritional rickets from 1998 to 2019. We observed a higher frequency of rickets in males (74 vs. 26%), in young children (median age at diagnosis: 23 months; 82% were younger than 5 years), and in children with a non-Caucasian ethnic background (89%). Most children were exclusively breastfed (78%) without adequate vitamin D supplementation (89%). The most common presentations were bowed legs (63%), hypocalcemic seizures (21%), and growth retardation (11%). Approximately half (62%) of the children were hypocalcemic. The children presenting with hypocalcemic seizures were significantly younger (0.8 vs. 2.2 years; p = 0.041) and had lower total serum calcium levels (1.44 vs. 2.17 mmol/L; p < 0.0001), higher phosphatemia (1.43 vs. 1.23 mmol/L; p = 0.020), and lower 25-hydroxy vitamin D levels (3 vs. 7 ng/mL; p = 0.020) but similar parathyroid hormone levels (357 vs. 289 ng/mL; p = 0.940) compared to rickets cases who did not experience hypocalcemic seizures. A dilated cardiomyopathy was detected in 14% of the children who had undergone echocardiography. Nutritional rickets remains endemic in the pediatric population and its most severe forms can have life-threatening sequelae. Health practitioners need to be cognizant of these facts to raise awareness and screen high-risk populations.

Identifiants

pubmed: 33120384
pii: 000511419
doi: 10.1159/000511419
doi:

Substances chimiques

Bone Density Conservation Agents 0
Vitamin D 1406-16-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

304-312

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Claire Flot (C)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Unité d'Endocrinologie, Maladies Osseuses et Génétique, Hôpital des Enfants, CHU de Toulouse, ERN BOND, INSERM UMR 1043/CNRS 5828, Université Paul Sabatier, Toulouse, France.

Valérie Porquet-Bordes (V)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Unité d'Endocrinologie, Maladies Osseuses et Génétique, Hôpital des Enfants, CHU de Toulouse, ERN BOND, INSERM UMR 1043/CNRS 5828, Université Paul Sabatier, Toulouse, France.

Justine Bacchetta (J)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Service de Néphrologie, Rhumatologie et Dermatologie Pédiatriques, Hôpital Femme Mère Enfant, INSERM UMR 1033, Bron, France.

Anya Rothenbuhler (A)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Endocrinology and Diabetology for Children, Hôpital Bicêtre Paris Saclay, Le Kremlin-Bicêtre, France.

Anne Lienhardt-Roussie (A)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Service de Pédiatrie, CHU de Limoges, Limoges, France.

Eloise Giabicani (E)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, APHP, Explorations Fonctionnelles Endocriniennes Hôpital Armand Trousseau, Paris, France.

Iva Gueorguieva (I)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Service d'Endocrinologie Pédiatrique Hôpital Jeanne de Flandres, CHR Lille, Lille, France.

Caroline Storey (C)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Département d'Endocrinologie et Diabétologie Pédiatrique, Hôpital Universitaire Robert-Debré, Paris, France.

Agnès Linglart (A)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Endocrinology and Diabetology for Children, Hôpital Bicêtre Paris Saclay, Le Kremlin-Bicêtre, France.

Jean-Pierre Salles (JP)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France.
Unité d'Endocrinologie, Maladies Osseuses et Génétique, Hôpital des Enfants, CHU de Toulouse, ERN BOND, INSERM UMR 1043/CNRS 5828, Université Paul Sabatier, Toulouse, France.

Thomas Edouard (T)

Reference and Competence Centers for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Diseases, Paris, France, edouard.t@chu-toulouse.fr.
Unité d'Endocrinologie, Maladies Osseuses et Génétique, Hôpital des Enfants, CHU de Toulouse, ERN BOND, INSERM UMR 1043/CNRS 5828, Université Paul Sabatier, Toulouse, France, edouard.t@chu-toulouse.fr.

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