The findings in paediatric obstetric brachial palsy differ from those in older patients: a suggested explanation

Citation
Jw. Vredeveld et al., The findings in paediatric obstetric brachial palsy differ from those in older patients: a suggested explanation, DEVELOP MED, 42(3), 2000, pp. 158-161
Citations number
12
Categorie Soggetti
Pediatrics,"Neurosciences & Behavoir
Journal title
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
ISSN journal
00121622 → ACNP
Volume
42
Issue
3
Year of publication
2000
Pages
158 - 161
Database
ISI
SICI code
0012-1622(200003)42:3<158:TFIPOB>2.0.ZU;2-O
Abstract
An EMG and nerve-conduction-study protocol has been developed and used in a ll patients with brachial plexus lesions since 1985, The findings of EMG an d nerve-conduction studies in obstetric brachial palsy (OBP) mostly suggest a falsely optimistic prognosis. To analyse this, all subjects were selecte d with complete avulsion of both roots C5 and C6 and/or complete rupture of the upper trunk verified during operation from a group of 162 infants with OBP (aged 4 to 14 months) and a group of 184 child and adult patients (age d 6 to 74 years) with a traumatic brachial plexus lesion. Fourteen infants, approximately 4 months old, with OBP, and 19 adults (aged 16 to 30 years) met the selection criteria. The infants from the group with OBP had at 4 mo nths a nearly normal recruitment pattern of motor units in the biceps brach ii and deltoid muscles, with little or no denervation, However, in the olde r group with traumatic brachial palsy, the same lesion caused complete dene rvation of both muscles. From the group with OBP, a third group (N=3) with the same lesion plus an additional lesion of Gr or a rupture of the middle trunk was selected. This additional lesion resulted in nearly complete dene rvation of both muscles. This means that C7 largely contributes to the inne rvation of both muscles at the time of birth, but this innervation is lost during later life in normally developing individuals (apoptosis), A central mechanism might be responsible for the clinical palsy and later spontaneou s improvement which is always found in the infants with OBP.