Dental approach to a pediatric patient with congenital insensitivity to pain and anhidrosis (CIPA) syndrome: A case report
Küçük Resim Yok
Tarih
2024
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier Ltd
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Congenital pain insensitivity syndrome with anhidrosis (CIPA, MIM 256800) or hereditary sensory and autonomic neuropathy (HSAN) type IV is a rare autosomal recessive disease. CIPA has characteristic symptoms such as failure to respond to painful stimuli, lack of thermal sensitivity, decreased or absent sweating (anhidrosis), varying degrees of reduced intellectual disability, musculoskeletal fractures, and joint deformities. A 4-year-old female patient diagnosed with CIPA syndrome presented to our clinic with the complaint of self-harm with her anterior teeth. In the clinical examination, sores were detected on the child's hands, fingers, mouth, and tongue. The front teeth of the patient, which caused the trauma, were extracted. In the 6-month follow-up, the patient's wounds healed. In this case report, the treatment of a patient with CIPA syndrome who was severely self-harming is described. © 2024 Japanese Society of Pediatric Dentistry
Açıklama
Anahtar Kelimeler
Congenital insensitivity to pain and anhidrosis (CIPA) syndrome, Hereditary sensory and autonomic neuropathy (HSAN) type IV, Lack of pain sensation, Pediatric patient, Tooth extraction
Kaynak
Pediatric Dental Journal
WoS Q Değeri
Scopus Q Değeri
Q2
