Page last updated: 2024-09-05

biotin and Xeroderma

biotin has been researched along with Xeroderma in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's2 (66.67)2.80

Authors

AuthorsStudies
Bennaoui, F; El Idrissi Slitine, N; El Moussaoui, S; Houcar, O; Maoulainine, FMR1
Cadieux-Dion, M; Gannon, J; Heese, B; Jenkins, J; Newell, B; Nopper, AJ; Saunders, C1
Anand, A; Chatterjee, A; Hiremagalore, R; Mani, RS; Pandey, N; Rajashekhar, B; Tharakan, A; Xavier, DF1

Other Studies

3 other study(ies) available for biotin and Xeroderma

ArticleYear
Biotinidase deficiency in a newborn.
    Journal of neonatal-perinatal medicine, 2020, Volume: 13, Issue:1

    Topics: Age of Onset; Alopecia; Biotin; Biotinidase Deficiency; Consanguinity; Dermatitis, Exfoliative; Eyebrows; Fatal Outcome; Health Services Accessibility; Humans; Ichthyosis; Infant, Newborn; Intensive Care Units, Neonatal; Male; Morocco; Muscle Hypotonia; Myoclonus; Rare Diseases; Vitamin B Complex

2020
Delayed diagnosis of holocarboxylase synthetase deficiency in three patients with prominent skin findings.
    Pediatric dermatology, 2021, Volume: 38, Issue:3

    Topics: Biotin; Delayed Diagnosis; Holocarboxylase Synthetase Deficiency; Humans; Ichthyosis; Seizures

2021
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.
    Annals of human genetics, 2016, Volume: 80, Issue:1

    Topics: Biotin; Connexin 30; Connexins; DNA Mutational Analysis; Female; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Ichthyosis; Keratoderma, Palmoplantar, Diffuse; Male; Pedigree; Phenotype; Skin Diseases, Genetic

2016