Hurler disease

Otology and Neurotology

Volumn 25, Issue 1, 2004, Pages 81-82

  Gocer, Celil ^a   Linthicum Jr , Fred H ^b,c  

^a ANKARA NUMUNE HOSPITAL   (Turkey)

^b HOUSE EAR INSTITUTE   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; COCHLEA FENESTRA; CONDUCTION DEAFNESS; FACIAL NERVE; FEMALE; GRANULATION TISSUE; HISTOPATHOLOGY; HUMAN; HURLER SYNDROME; PERCEPTION DEAFNESS; PRIORITY JOURNAL; TEMPORAL BONE; CHILD; DWARFISM; DYSOSTOSIS; ENZYMOLOGY; FATALITY; HEARING IMPAIRMENT; MENTAL DEFICIENCY; MICROPHOTOGRAPHY; PATHOLOGY; PATHOPHYSIOLOGY;

LEVO IDURONIDASE;

CHILD; DEAFNESS; DWARFISM; DYSOSTOSES; FATAL OUTCOME; FEMALE; HUMANS; IDURONIDASE; MENTAL RETARDATION; MUCOPOLYSACCHARIDOSIS I; PHOTOMICROGRAPHY; TEMPORAL BONE;

EID: 2342442137     PISSN: 15317129     EISSN: None     Source Type: Journal    
DOI: 10.1097/00129492-200401000-00016     Document Type: Article

References (3)

1. Friedmann I, Arnold W. Pathology of the Ear. New York: Churchill Livingstone, 1993.
2. Shea DA, Schachem PA, Paparella MM. Mucopolysaccharidosis I-H (Hurler's syndrome) and human temporal bone histopathology. Ann Otol Rhinol Laryngol 1984;93:65-9.
3. Friedmann I, Spellacy E, Crowe J, Watts RWE. Histopathologic studies of the temporal bones in Hurler's disease (mucopolysaccharidosis). J Laryngol Otol 1984;99:29-41.