Author/Authors :
OFLUOĞLU, Duygu Istanbul University - Faculty of Dentistry - Department of Oral and Maxillofacial Surgery, Turkey , ALTIN, Nazlı Istanbul Aydın University - Faculty of Dentistry - Department of Oral and Maxillofacial Surgery, Turkey , YAMAN, Elif Istanbul University - Faculty of Dentistry - Department of Pedodontics, Turkey , TUNA-İNCE, Elif Bahar Istanbul University - Faculty of Dentistry - Department of Pedodontics, Turkey , AYTEPE, Zeynep Istanbul University - Faculty of Dentistry - Department of Pedodontics, Turkey , TANYERİ, Hakkı Istanbul University - Faculty of Dentistry - Department of Oral and Maxillofacial Surgery, Turkey
Abstract :
Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic syndromes of unknown etiology. They are seen in early childhood and are categorized into six different types by their symptoms. HSAN type 4 demonstrates autosomal recessive transmission pattern, with such major characteristics as loss of sense of pain, self-mutilation, anhydrosis and mental retardation. Sympathetic innervations are deficient despite the existence of sweat glands. Sufferers are hypotonic without any tendon reflexes, and neuro-motor development is retarded. In some cases tactile sensation and vibration may be intact. Biting injuries due to lack of pain sensation cause laceration, ulceration and scarring of the tongue, lips and other parts of oral mucosa. Tooth luxation and severe dental attrition have been observed. This case report presents oral and dental findings, surgical treatments and prosthetic rehabilitation of an 11-year-old boy with HSAN type 4.
Keywords :
Hereditary sensory and autonomic neuropathy , Type IV , Dental needs , Removable partial prosthesis