SynthesisClinical oral investigations2013
Dental and oral anomalies in incontinentia pigmenti: a systematic review.
Synthesis in Clinical oral investigations, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.
What it found
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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.
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.
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Who cites it
18 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.
- Systematic review of central nervous system anomalies in incontinentia pigmenti.Orphanet journal of rare diseases · 2013Pooled it
- A case of Incontinentia Pigmenti associated with concurrentFrontiers in medicine · 2026Article
- Ectodermal dysplasia: a narrative review of the clinical and biological aspects relevant to oral health.Frontiers in pediatrics · 2025Review
- Case report: Variability in clinical manifestations within a family with incontinentia pigmenti.Frontiers in medicine · 2024Article
- The Impact of theDiagnostics (Basel, Switzerland) · 2023Article
- Avascular Peripheral Retina in Infants.Turkish journal of ophthalmology · 2023Review
- Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male.International journal of molecular sciences · 2022Review
- NEMO Gene Mutations in Two Chinese Females with Incontinentia Pigmenti.Clinical, cosmetic and investigational dermatology · 2022Article
- Incontinentia Pigmenti: A Case Report of a Complex Systemic Disease.Open access Macedonian journal of medical sciences · 2017Article
- The epidemiology of supernumerary teeth and the associated molecular mechanism.Organogenesis · 2017Review
- Dental anomalies in 14 patients with IP: clinical and radiological analysis and review.Clinical oral investigations · 2017Article
- Incontinentia Pigmenti; a Rare Multisystem Disorder: Case Report of a 10-Year-Old Girl.Journal of dentistry (Shiraz, Iran) · 2016Article
- A Multidisciplinary Approach to a Seven Year-Old Patient with Incontinentia Pigmenti: A Case Report and Five-Year Follow Up.Journal of dentistry (Tehran, Iran) · 2016Article
- Reticulated, Hyperchromic Rash in a Striated Pattern Mimicking Atopic Dermatitis and Fungal Infection in a 2-Month-Old Female: A Case of Incontinentia Pigmenti.Case reports in pediatrics · 2016Article
- Incontinentia pigmenti.Anais brasileiros de dermatologiaReview
- Ectodermal Dysplasia - An Overview and Update.Indian dermatology online journalReview
- Dental treatment considerations for a pediatric patient with incontinentia pigmenti (Bloch-Sulzberger syndrome).European journal of dentistryArticle
- Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis.Anais brasileiros de dermatologiaArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectivesIncontinentia pigmenti (IP) is an X-linked genodermatosis caused by a mutation of the IKBKG gene. The objective of this study was to present a systematic review of the dental and oral types of anomalies, to determine the total number and sex distribution of the anomalies, and to analyze possible therapies. MATERIALS AND
methodsWe analyzed the literature data from 1,286 IP cases from the period 1993-2010.
resultsDental and/or oral anomalies were diagnosed for 54.38% of the investigated IP patients. Most of the anomaly types were dental, and the most frequent of these were dental shape anomalies, hypodontia, and delayed dentition. The most frequent oral anomaly types were cleft palate and high arched palate. IKBKG exon 4-10 deletion was present in 86.36% of genetically confirmed IP patients.
conclusionsAccording to the frequency, dental and/or oral anomalies represent the most frequent and important IP minor criteria. The most frequent mutation was IKBKG exon 4-10 deletion. The majority of dental anomalies and some of the oral anomalies could be corrected. CLINICAL RELEVANCE: Because of the presence of cleft palate and high arched palate in IP patients, these two anomalies may be considered as diagnostic IP minor criteria as well.
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Registered trials
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.