Evidence map›Paper›PMID 36656330›Full record

SynthesisCalcified tissue international2023

Vitamin D-Dependent Rickets Type 3: A Case Report and Systematic Review.

Lucas Mantoanelli, Camila Medeiros de Almeida, Maria Caroline Alves Coelho, Marcelo Coutinho, Michael A Levine, Paulo Ferrez Collett-Solberg, Ana Paula Bordallo

Open access · greenAbstract readCase ReportsSystematic Review
In one paragraph

Synthesis in Calcified tissue international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Approach to Rickets: Is It Calciopenic or Phosphopenic?Turkish archives of pediatrics · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Lucas MantoanelliFaculdade de Ciências Médicas, Departamento de Medicina Interna, Universidade do Estado do Rio de Janeiro, Serviço de Endocrinologia, Rio de Janeiro, RJ, Brazil.
Camila Medeiros de AlmeidaFaculdade de Ciências Médicas, Departamento de Medicina Interna, Universidade do Estado do Rio de Janeiro, Serviço de Endocrinologia, Rio de Janeiro, RJ, Brazil.
Maria Caroline Alves CoelhoFaculdade de Ciências Médicas, Departamento de Medicina Interna, Universidade do Estado do Rio de Janeiro, Serviço de Endocrinologia, Rio de Janeiro, RJ, Brazil.
Marcelo CoutinhoFaculdade Metropolitana São Carlos, Medical Genetics Unit, Campos de Goytacazes, RJ, Brazil.
Michael A LevineCenter for Bone Health at the Children's Hospital of Philadelphia and Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA. levinem@chop.edu.
Paulo Ferrez Collett-SolbergFaculdade de Ciências Médicas, Departamento de Medicina Interna, Universidade do Estado do Rio de Janeiro, Serviço de Endocrinologia, Rio de Janeiro, RJ, Brazil.
Ana Paula BordalloFaculdade de Ciências Médicas, Departamento de Medicina Interna, Universidade do Estado do Rio de Janeiro, Serviço de Endocrinologia, Rio de Janeiro, RJ, Brazil.
Universidade do Estado do Rio de Janeiro · BRUniversity of Pennsylvania · US

Funding

Repurposing rifampin to reduce elevated levels of blood and urine calcium in patients with inactivating mutations of CYP24A1R01DK112955 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI Michael A. Levine, David R Weber · 2017 to 2026
$5.1M
NIDDK NIH HHS R01 DK112955
6 · The paper itself

Abstract

Although vitamin D deficiency resulting from insufficient sunlight exposure or inadequate dietary vitamin D intake is the most common cause of rickets, mutations in genes involved in vitamin D metabolism can cause genetic forms of rickets termed Vitamin D-Dependent Rickets (VDDR). In 2018, Roizen et al. described a new type of VDDR, named VDDR3, caused by a recurrent missense mutation in the CYP3A4 gene that leads to accelerated inactivation of vitamin D metabolites. Here, we describe the third case of VDDR3 due to the same CYP3A4 mutation in a 2-year-old boy with bone deformities associated with poor growth. As in the previously reported cases, this patient had no family history of rickets. Serial measurements of vitamin D metabolites after a single 150,000 IU dose of cholecalciferol demonstrated an accelerated inactivation of 25(OH)D and 1,25(OH)2D. Significant improvement in growth velocity and healing of bone deformities were achieved after a short period of treatment with 10.000 IU of cholecalciferol daily, showing the importance of early recognition and prompt precision therapy of this condition.

Indexed as

RicketsVitamin D DeficiencyChild, PreschoolCholecalciferolCytochrome P-450 CYP3AHumansMaleVitamin DCholecalciferolCytochrome P-450 CYP3AVitamin DCYP3A4 geneRicketsVitamin DVitamin D-dependent rickets

Identifiers

PMID36656330
PMCPMC10393508
OpenAlexW4317435582

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.