Details

Autor(en) / Beteiligte

• Bar, C
• Villéga, F
• Espil, C
• Husson, M
• Pedespan, J-M
• Rouanet, M-F

Titel

Hereditary neuropathy with liability to pressure palsies in childhood: Report of three cases

Ist Teil von

• Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2017-03, Vol.24 (3), p.260-262

Ort / Verlag

France

Erscheinungsjahr

2017

Quelle

MEDLINE

Beschreibungen/Notizen

• Hereditary neuropathy with liability to pressure palsy (HNPP) is an autosomal dominant neuropathy. It is characterized by recurrent sensory and motor nerve palsies, usually precipitated by minor trauma or compression. Even though rare in childhood, this disorder is probably underdiagnosed given its wide spectrum of clinical symptoms. We review three separate cases of HNPP diagnosed in children with various phenotypes: fluctuating and distal paresthesias disrupting learning at school, cramps related to intensive piano practice, and discrete muscle weakness with no functional complaint. Family history should be carefully reviewed to identify potential undiagnosed HNPP cases, as in our three reports. Electrophysiological study is essential for the diagnosis, with a double advantage: to confirm the presence of focal abnormalities in clinically symptomatic areas and to guide molecular biology by revealing an underlying demyelinating polyneuropathy. The diagnosis of HNPP is confirmed by genetic testing, which in 90% of cases shows a 1.5-Mb deletion of chromosome 17p11.2 including the PMP22 gene. Patients are expected to make a full recovery after each relapse. However, it is very important for both the patient and his or her family to establish a diagnosis in order to prevent recurrent palsy brought on by situations involving prolonged immobilizations leading to nerve compression.