Orphanet Journal of Rare Diseases · 2020 · 19 citations · 21 references
DentistryImmunologyPediatric DentistryAllergyHypersensitivityOral ImmunologyAllergic ConditionsAtopic DermatitisOral CareOral Health Outcomes ResearchPediatric Oral HealthType I HypersensitivityAtopic Dermatitis AssociationEarly Intervention InclusionEarly Intervention RegimesHyper-ige SyndromeMidline Craniofacial DefectsOral Hypersensitivity ReactionsPediatric Atopic DermatitisPrimary Immunodeficiency Disorders
BACKGROUND: STAT3 hyper-IgE syndrome (STAT3-HIES) is a rare primary immunodeficiency that clinically overlaps with atopic dermatitis. In addition to eczema, elevated serum-IgE, and recurrent infections, STAT3-HIES patients suffer from characteristic facies, midline defects, and retained primary teeth. To optimize dental management we assessed the development of dentition and the long-term outcomes of dental treatment in 13 molecularly defined STAT3-HIES patients using questionnaires, radiographs, and dental investigations. RESULTS: Primary tooth eruption was unremarkable in all STAT3-HIES patients evaluated. Primary tooth exfoliation and permanent tooth eruption was delayed in 83% of patients due to unresorbed tooth roots. A complex orthodontic treatment was needed for one patient receiving delayed extraction of primary molars and canines. Permanent teeth erupted spontaneously in all patients receiving primary teeth extraction of retained primary teeth during average physiologic exfoliation time. CONCLUSIONS: The association of STAT3-HIES with retained primary teeth is important knowledge for dentists and physicians as timely extraction of retained primary teeth prevents dental complications. To enable spontaneous eruption of permanent teeth in children with STAT3-HIES, we recommend extracting retained primary incisors when the patient is not older than 9 years of age and retained primary canines and molars when the patient is not older than 13 years of age, after having confirmed the presence of the permanent successor teeth by radiograph.
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<i>STAT3</i> Mutations in the Hyper-IgE Syndrome
Steven M. Holland, Frank R. DeLeo, Houda Zghal Elloumi et al. · New England Journal of Medicine · 2007 · 1.2K citations · Full text
Life Sciences, Genetics, Immunology +13
Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
Joshua D. Milner, Jason M. Brenchley, Arian Laurence et al. · Nature · 2008 · 1.1K citations · Full text
Life Sciences, Genetics, Immunology +14
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
Yoshiyuki Minegishi, Masako Saitō, Shigeru Tsuchiya et al. · Nature · 2007 · 1K citations
Life Sciences, Genetics, Immunology +13