Pelizaeus-Merzbacher disease (PMD) is a rare dysmyelinating disorder of the CNS. The cause is abnormal production of proteolipid protein–1 (PLP-1 )that is a principal components of myelin. It is characterised by rotatory nistagmus, early muscular hypotonia, head shake, ataxia, spasticity and mental retardation. The diagnosis of PMD is with clinical findings, MRI and genetic analysis. MR spectroscopy findings of PMD show differences. However the MR spectroscopy may be helpful in the diagnosis and differential diagnosis of PMD. In this article, a case with PMD and MRS findings is reported in light of the literature. Key words: Pelizaeus-Merzbacher Disease, Magnetic Resonance, Spectroscopy
Spalice A, Popolizio T, Parisi P, et al. Proton MR spectroscopy in connatal Pelizaeus-Merzbacher disease. Pediatr Radiol 2000; 30: 171-5.
Wang PJ, Hwu WL, Lee WT, Wang TR, et al. Duplication of proteolipid protein gene: a possible major cause of Pelizaeus- Merzbacher disease. Pediatr Neurol 1997; 17: 125-8.
Inoue K, Osaka H, Imaizumi K, et al. Proteolipid protein gene duplication causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestations. Ann Neurol 1999; 45: 624-32.
Boesplug-Tanguy O, Mimault C, Melki J, et al. Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. Am J Hum Genet 1994; 55: 461-7.
Begleiter MI, Haris DJ. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease. Am J Med Genet 1989; 33: 311-3.
Nezu A, Kimura S, Uehara S, et al. Pelizaeus-Merzbacher-like disease: female case report. Brain Dev 1996; 18: 114-8.
Takanashi J, Inoue K, Tomita M, et al. Brain N-acetylaspartate is elevated in Pelizaeus-Merzbacher disease with PLP1 duplication. Neurology 2002; 58: 237-41.
Boulloche J, Aicardi J. Pelizaeus-Merzbacher disease: clinical and nosological study. J Child Neurol 1986; 1: 233-9.
Sistermans EA, de Coo RFM, De Wijs IJ, et al. Duplication of proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease. Neurology 1998; 50: 1749-54.
Mader I, Roser W, Kappos L, et al. Serial proton MR spectroscopy of contrast-enhancing multiple sclerosis plaques: absolute metabolic values over 2 years during a clinical pharmacological study. Am J Neuroradiol 2000; 21: 1220-7.
Suhy J, Rooney WD, Googkin DE, et al. 1H MRSI comparison of white matter and lesions in primary progressive and relapsing- remitting MS. Mult Scler 2000; 6: 148-55.
Takanashi J, Sugita K, Ishii M, et al. Evaluation of Pelizaeus- Merzbacher disease with proton magnetic resonance spectroscopy. Am J Neuroradiol 1997; 18: 533-5.
Bonavita S, Schiffmann R, Moore DF, et al. Evidence for neuroaxonal injury in patients with proteolipid protein gene mutation. Neurology 2001;56: 785-8.
Pelizaeus-Merzbacher hastalığı (PMH) SSS'nin nadir görülen bir dismiyelinizan bozukluğu olup, miyelinin temel komponentlerinden biri olan proteolipit protein-1 üretimindeki anormallik sonucu oluşur. Rotatuar nistagmus, kas hipotonisi, baş sallama, ataksi, spastisite ve zeka geriliği ile karakterizedir. Tanı klinik, genetik ve manyetik rezonans görüntüleme (MRG) bulguları ile birlikte konulur. MR spektroskopi bulguları ise farklılık göstermektedir. Ancak PMH'nin tanı ve ayırıcı tanısında manyetik rezonans spektroskopi (MRS) yardımcı bir tanı yöntemi olarak kullanılabilir. Bu makalede PMH'li bir vaka ve MRS bulguları literatür bilgileri ışığında sunulmuştur. Anahtar kelimeler: Pelizaeus-Merzbacher Hastalığı, Manyetik Rezonans, Spektroskopi
Spalice A, Popolizio T, Parisi P, et al. Proton MR spectroscopy in connatal Pelizaeus-Merzbacher disease. Pediatr Radiol 2000; 30: 171-5.
Wang PJ, Hwu WL, Lee WT, Wang TR, et al. Duplication of proteolipid protein gene: a possible major cause of Pelizaeus- Merzbacher disease. Pediatr Neurol 1997; 17: 125-8.
Inoue K, Osaka H, Imaizumi K, et al. Proteolipid protein gene duplication causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestations. Ann Neurol 1999; 45: 624-32.
Boesplug-Tanguy O, Mimault C, Melki J, et al. Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. Am J Hum Genet 1994; 55: 461-7.
Begleiter MI, Haris DJ. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease. Am J Med Genet 1989; 33: 311-3.
Nezu A, Kimura S, Uehara S, et al. Pelizaeus-Merzbacher-like disease: female case report. Brain Dev 1996; 18: 114-8.
Takanashi J, Inoue K, Tomita M, et al. Brain N-acetylaspartate is elevated in Pelizaeus-Merzbacher disease with PLP1 duplication. Neurology 2002; 58: 237-41.
Boulloche J, Aicardi J. Pelizaeus-Merzbacher disease: clinical and nosological study. J Child Neurol 1986; 1: 233-9.
Sistermans EA, de Coo RFM, De Wijs IJ, et al. Duplication of proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease. Neurology 1998; 50: 1749-54.
Mader I, Roser W, Kappos L, et al. Serial proton MR spectroscopy of contrast-enhancing multiple sclerosis plaques: absolute metabolic values over 2 years during a clinical pharmacological study. Am J Neuroradiol 2000; 21: 1220-7.
Suhy J, Rooney WD, Googkin DE, et al. 1H MRSI comparison of white matter and lesions in primary progressive and relapsing- remitting MS. Mult Scler 2000; 6: 148-55.
Takanashi J, Sugita K, Ishii M, et al. Evaluation of Pelizaeus- Merzbacher disease with proton magnetic resonance spectroscopy. Am J Neuroradiol 1997; 18: 533-5.
Bonavita S, Schiffmann R, Moore DF, et al. Evidence for neuroaxonal injury in patients with proteolipid protein gene mutation. Neurology 2001;56: 785-8.
Aslan, M., Doğan, M., Doğan, D. G., … Yakıncı, C. (2009). Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu. Journal of Turgut Ozal Medical Center, 16(4), 265-268.
AMA
Aslan M, Doğan M, Doğan DG, Yakıncı C, Alkan A. Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu. J Turgut Ozal Med Cent. Ağustos 2009;16(4):265-268.
Chicago
Aslan, Mehmet, Metin Doğan, Derya Gümüş Doğan, Cengiz Yakıncı, ve Alpay Alkan. “Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu”. Journal of Turgut Ozal Medical Center 16, sy. 4 (Ağustos 2009): 265-68.
EndNote
Aslan M, Doğan M, Doğan DG, Yakıncı C, Alkan A (01 Ağustos 2009) Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu. Journal of Turgut Ozal Medical Center 16 4 265–268.
IEEE
M. Aslan, M. Doğan, D. G. Doğan, C. Yakıncı, ve A. Alkan, “Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu”, J Turgut Ozal Med Cent, c. 16, sy. 4, ss. 265–268, 2009.
ISNAD
Aslan, Mehmet vd. “Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu”. Journal of Turgut Ozal Medical Center 16/4 (Ağustos2009), 265-268.
JAMA
Aslan M, Doğan M, Doğan DG, Yakıncı C, Alkan A. Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu. J Turgut Ozal Med Cent. 2009;16:265–268.
MLA
Aslan, Mehmet vd. “Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu”. Journal of Turgut Ozal Medical Center, c. 16, sy. 4, 2009, ss. 265-8.
Vancouver
Aslan M, Doğan M, Doğan DG, Yakıncı C, Alkan A. Pelizaeus-Merzbacher Hastalığı ve MR-Spektroskopi Bulguları: Vaka Sunumu. J Turgut Ozal Med Cent. 2009;16(4):265-8.