Stable motor and lung function throughout pregnancy in a patient with infantile spinal muscular atrophy type II

Neuromuscular Disorders

Volumn 12, Issue 2, 2002, Pages 137-140

  Rudnik Schöneborn, Sabine ^a   Breuer, Christian ^a   Zerres, Klaus ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Lung function; Pregnancy; Proximal spinal muscular atrophy

Indexed keywords

ADULT; ARTERIAL CARBON DIOXIDE TENSION; ARTICLE; BLOOD GAS; CASE REPORT; CESAREAN SECTION; DELIVERY; DYSPNEA; FATIGUE; FEMALE; FORCED EXPIRATORY VOLUME; GESTATIONAL AGE; HEREDITARY SPINAL MUSCULAR ATROPHY; HUMAN; HYPERVENTILATION; LUNG FUNCTION; MOTOR PERFORMANCE; OXYGEN TENSION; PREGNANCY; PREGNANCY COMPLICATION; PRIORITY JOURNAL; PROSPECTIVE STUDY;

ADULT; CARBON DIOXIDE; DELIVERY, OBSTETRIC; FEMALE; HUMANS; INFANT, NEWBORN; MALE; MOTOR ACTIVITY; OXYGEN; PARTIAL PRESSURE; PREGNANCY; PREGNANCY COMPLICATIONS; PREGNANCY OUTCOME; PUERPERAL DISORDERS; RESPIRATORY FUNCTION TESTS; SPINAL MUSCULAR ATROPHIES OF CHILDHOOD; SPIROMETRY;

EID: 0036133348     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(01)00271-1     Document Type: Article

References (11)

1. Workshop report
2. Successful pregnancies in the presence of spinal muscular atrophy: Two case reports
3. Pregnancy and delivery in case of chronic anterior horn cell disease
4. Association of Werdnig-Hoffmann disease and gestation: An unusual case
5. Pregnancy and delivery in a woman with neuromuscular disease. Spinal muscular atrophy and severely reduced pulmonary function
6. Successful pregnancy and spinal muscular atrophy
7. Pregnancy and spinal muscular atrophy
8. A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 Patients
9. Clinical and genetic study of chronic (types II and III) childhood onset spinal muscular atrophy
10. Cardio-respiratory physiological adaptation of pregnancy
11. Pulmonary manifestations of neuromuscular disease with special reference to Duchenne muscular dystrophy and spinal muscular atrophy