Congenital insensitivity to pain and anhydrosis due to a rare mutation and that is complicated by inflammatory bowel disease and amyloidosis: a case report.

Bakri, Faris G; Wahbeh, Ayman; Abu Sneina, Awni; Al Khader, Ali; Obeidat, Fatima; AlAwwa, Izzat; Buni, Maryam; Ki, Chang-Seok; Masri, Amira

Bakri, Faris G; Wahbeh, Ayman; Abu Sneina, Awni; Al Khader, Ali; Obeidat, Fatima; AlAwwa, Izzat; Buni, Maryam; Ki, Chang-Seok; Masri, Amira.

Afiliación

Bakri FG; Department of Medicine School of Medicine The University of Jordan Amman Jordan.
Wahbeh A; Department of Medicine School of Medicine The University of Jordan Amman Jordan.
Abu Sneina A; Department of Medicine School of Medicine The University of Jordan Amman Jordan.
Al Khader A; Department of Laboratory Medicine Division of Pathology Jordan University Hospital The University of Jordan Amman Jordan.
Obeidat F; Department of Laboratory Medicine Division of Pathology Jordan University Hospital The University of Jordan Amman Jordan.
AlAwwa I; Department of Medicine School of Medicine The University of Jordan Amman Jordan.
Buni M; Internal Medicine Residency Training Program Department of Internal Medicine University of Texas Medical School at Houston Houston Texas USA.
Ki CS; Department of Laboratory Medicine & Genetics Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Korea.
Masri A; Department of Pediatrics Division of Child Neurology Jordan University Hospital The University of Jordan Amman Jordan.

Clin Case Rep ; 4(10): 997-1000, 2016 Oct.

Article en En | MEDLINE | ID: mdl-27761255

ABSTRACT

ABSTRACT

Patients with congenital insensitivity to pain and anhydrosis syndrome are at risk for renal amyloidosis and inflammatory bowel disease. Physicians caring for such patients should be aware of these complications.

Palabras clave

Amyloidosis; Jordan; NTRK1 gene; congenital insensitivity to pain and anhydrosis; hereditary sensory and autonomic neuropathy; inflammatory bowel disease; nephrotic syndrome; osteomyelitis

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2016 Tipo del documento: Article