TY - JOUR
T1 - Correction of blepharoptosis in oculopharyngeal muscular dystrophy
AU - Kang, Dong Hee
AU - Koo, Sang Hwan
AU - Ahn, Duck Sun
AU - Park, Seung Ha
AU - Yoon, Eul Sik
PY - 2002/10/1
Y1 - 2002/10/1
N2 - Oculopharyngeal muscular dystrophy is a hereditary, autosomal dominant, slowly progressive disorder with onset that occurs during middle age. Major symptoms are ptosis and dysphagia resulting primarily from selectively involved levator palpebrae and the pharyngeal muscles. Progressive, usually symmetrical blepharoptosis, with or without dysphagia, appears during middle age. Muscular weakness in the limbs can be noted in some patients. The guidelines for surgery in myopathic ptosis are conservative in view of the increased risk of postoperative corneal complications. However, orbicularis function remains intact in oculopharyngeal muscular dystrophy; therefore, corrective surgery is performed in most patients. This report describes four cases of ptosis correction in patients with oculopharyngeal muscular dystrophy in one family. The frontalis action was very poor to qualify for frontalis transfer; therefore, the authors performed moderate to large levator resection in all patients. The follow-up results 5 years postoperatively are promising to date and all the patients are satisfied with the results.
AB - Oculopharyngeal muscular dystrophy is a hereditary, autosomal dominant, slowly progressive disorder with onset that occurs during middle age. Major symptoms are ptosis and dysphagia resulting primarily from selectively involved levator palpebrae and the pharyngeal muscles. Progressive, usually symmetrical blepharoptosis, with or without dysphagia, appears during middle age. Muscular weakness in the limbs can be noted in some patients. The guidelines for surgery in myopathic ptosis are conservative in view of the increased risk of postoperative corneal complications. However, orbicularis function remains intact in oculopharyngeal muscular dystrophy; therefore, corrective surgery is performed in most patients. This report describes four cases of ptosis correction in patients with oculopharyngeal muscular dystrophy in one family. The frontalis action was very poor to qualify for frontalis transfer; therefore, the authors performed moderate to large levator resection in all patients. The follow-up results 5 years postoperatively are promising to date and all the patients are satisfied with the results.
UR - http://www.scopus.com/inward/record.url?scp=0036789505&partnerID=8YFLogxK
U2 - 10.1097/00000637-200210000-00015
DO - 10.1097/00000637-200210000-00015
M3 - Article
C2 - 12370650
AN - SCOPUS:0036789505
SN - 0148-7043
VL - 49
SP - 419
EP - 423
JO - Annals of Plastic Surgery
JF - Annals of Plastic Surgery
IS - 4
ER -