A case of mid‐face toddler excoriation syndrome (MiTES)
Author:
Affiliation:
1. Department of Dermatology Hospital Universitario Infantil Niño Jesús Madrid Spain
2. Department of Genetis Hospital Universitario Infantil Niño Jesús Madrid Spain
3. Department of Dermatology Hospital Universitario Gregorio Marañón Madrid Spain
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14081
Reference4 articles.
1. Transcriptional regulator PRDM12 is essential for human pain perception
2. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature
3. Mid-face toddler excoriation syndrome (MiTES): a new paediatric diagnosis
4. Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12
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1. Midfacial toddler excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism;British Journal of Dermatology;2024-04-09
2. Neurological Conditions Affecting the Skin;Rook's Textbook of Dermatology;2024-03-19
3. Midface Toddler Excoriation Syndrome – A Tale of Scarring Excoriation of the Face;Indian Journal of Paediatric Dermatology;2023
4. Prdm12, a key transcriptional regulator of the nociceptive lineage;The Neurobiology, Physiology, and Psychology of Pain;2022
5. PRDM12 in Health and Diseases;International Journal of Molecular Sciences;2021-11-06
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