Congenital Insensitivity to Pain and Anhydrosis: A Report of Two Cases
نویسندگان
چکیده
منابع مشابه
Congenital insensitivity to pain and anhydrosis: a report of two cases.
We report on 2 patients with congenital insensitivity to pain and anhydrosis. The first one was a 7-month-old boy who presented with non-traumatic, haematogenous septic dislocation of the right elbow with physeal separation of the distal humerus. The second one was a 3-year-old girl suspected to have Job syndrome with an altered immunological profile.
متن کامل[Congenital insensitivity to pain with anhydrosis].
Congenital insensitivity to pain with anhydrosis (CIPA) is a rare genetic disorder characterized by inability to feel pain and temperature, and decreased or absent sweating. Familiarity to this condition is important to avoid misdiagnosing it with leprosy and other peripheral nerve diseases. An inability to feel pain may lead to repeated self-trauma (tongue, lips and finger tips) ultimately lea...
متن کاملCongenital Insensitivity to Pain and Anhydrosis (CIPA) Syndrome; A Report of 4 Cases
BACKGROUND BACKGROUND Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of infections and unexplained fever, anhidrosis (inability to sweat), and absence of reaction to noxious stimuli, self-mutilating behavior, mental retardation and damages to oral structures. CASE PRESENTATION In this article, we have demonstrated the signs and symptoms of 4 ...
متن کاملCongenital insensitivity to pain with anhydrosis: report of a family case
Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classified as hereditary sensory and autonomic neuropathy type IV. Pain insensitivity and autonomic deficits are present, but touch and pressure sensitivity are unimpaired. Mental retardation is usually present. We report a family case of a 5 years old girl and 2 years old boy with congenital insensitivit...
متن کاملCase Report: Congenital Insensitivity to Pain
Congenital Insensitivity to Pain belongs to the family of Hereditary Sensory and Autonomic Neuropathies (HSAN). It is a rare disorder of unknown etiology associated with loss of pain sensation. Cognition and sensation is otherwise normal and there is no detectable physical abnormality. We report a case of Congenital Insensitivity to Pain in a 3 year old female child.
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ژورنال
عنوان ژورنال: Journal of Orthopaedic Surgery
سال: 2013
ISSN: 2309-4990,2309-4990
DOI: 10.1177/230949901302100132