Progressive infantile axonal polyneuropathy

Journal of Child Neurology

Volumn 15, Issue 8, 2000, Pages 513-517

  Geller, Thomas J ^a   Connolly, Anne M ^b   Kotagal, Suresh ^a   Prensky, Arthur L ^b  

^a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; ELECTROPHYSIOLOGY; FAMILIAL DISEASE; GENETIC ANALYSIS; HUMAN; INFANT; MALE; ONSET AGE; POLYNEUROPATHY; PRESCHOOL CHILD; PRIORITY JOURNAL; QUADRIPLEGIA; SENSORIMOTOR NEUROPATHY; SPINAL MUSCULAR ATROPHY;

AGE OF ONSET; AXONS; BIOPSY; ELECTROPHYSIOLOGY; FATAL OUTCOME; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; INFANT; MALE; MUSCLE, SKELETAL; QUADRIPLEGIA; RESPIRATION, ARTIFICIAL; RESPIRATORY INSUFFICIENCY; SPINAL CORD; SURAL NERVE;

EID: 0033849504     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380001500804     Document Type: Article

References (11)

1. Congenital hypomyelinating neuropathy: Two patients with long-term follow-up
2. Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood
3. Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathy
4. Nerve conduction studies in infants and children
5. Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region
6. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy
7. Vocal cord paralysis as a presenting sign of acute spinal muscular atrophy (SMA) type 1
8. Congenital peripheral neuropathy presenting as apnoea and respiratory insufficiency
9. Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis
10. Infantile axonal neuropathy in two siblings