Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy

被引:94
|
作者
Friedman, Jennifer [1 ,2 ,3 ]
Roze, Emmanuel [4 ,5 ,6 ]
Abdenur, Jose E. [7 ]
Chang, Richard [7 ]
Gasperini, Serena [8 ,9 ]
Saletti, Veronica [10 ]
Wali, Gurusidheshwar M. [11 ]
Eiroa, Hernan [12 ]
Neville, Brian [13 ]
Felice, Alex [14 ]
Parascandalo, Ray [15 ]
Zafeiriou, Dimitrios I. [16 ]
Arrabal-Fernandez, Luisa [17 ]
Dill, Patricia [18 ]
Eichler, Florian S. [19 ]
Echenne, Bernard [20 ]
Gutierrez-Solana, Luis G. [21 ]
Hoffmann, Georg F. [22 ]
Hyland, Keith [23 ]
Kusmierska, Katarzyna [24 ]
Tijssen, Marina A. J. [25 ]
Lutz, Thomas [22 ]
Mazzuca, Michel [26 ,27 ]
Penzien, Johann [28 ]
Bwee Tien Poll-The [29 ]
Sykut-Cegielska, Jolanta [30 ]
Szymanska, Krystyna [31 ]
Thoeny, Beat [32 ,33 ]
Blau, Nenad [22 ,32 ,33 ]
机构
[1] Rady Childrens Hosp, 8010 Frost St,Suite 400, San Diego, CA 92123 USA
[2] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[4] Salpetriere Hosp, APHP, Dept Neurol, Paris, France
[5] Salpetriere Hosp, INSERM, UMRS 975, Paris, France
[6] Salpetriere Hosp, CNRS CRICM 7225, Paris, France
[7] Childrens Hosp Orange Cty, Orange, CA 92668 USA
[8] Univ Florence, Anna Meyer Childrens Hosp, Pediat Neurol Unit, Dept Neurosci, Florence, Italy
[9] Univ Florence, Anna Meyer Childrens Hosp, Metab & Neuromuscular Disorders Unit, Dept Neurosci, Florence, Italy
[10] IRCCS Fdn, Carlo Besta Neurol Inst, Dev Neurol Unit, Milan, Italy
[11] Neurospecial Ctr, Belgaum, India
[12] Hosp Pediat JP Garrahan, Serv Errores Congenitos Metab, Buenos Aires, DF, Argentina
[13] UCL, Inst Child Hlth, Neurosci Unit, London, England
[14] Univ Malta, Fac Med & Surg, Dept Physiol & Biochem, Mol Genet Lab, Msida, Malta
[15] Mater Dei Hosp, Dept Pediat, Valletta, Malta
[16] Aristotle Univ Thessaloniki, Dept Pediat 1, GR-54006 Thessaloniki, Greece
[17] Virgen de las Nieves Hosp, Dept Pediat, Granada, Spain
[18] Univ Childrens Hosp, Div Pediat Neurol & Dev Med, Basel, Switzerland
[19] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Child Neurol, Boston, MA USA
[20] Gui de Chauliac Hosp, Dept Pediat Neurol, Montpellier, France
[21] Hosp Infantil Univ Nino Jesus, Secc Neurol, Madrid, Spain
[22] Univ Childrens Hosp Heidelberg, Heidelberg, Germany
[23] Med Neurogenet, Atlanta, GA USA
[24] Childrens Mem Hlth Inst, Dept Biochem & Expt Med, Lab Metab Disorders, Warsaw, Poland
[25] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
[26] Univ Lyon 1, INSERM, U1028, CNRS,UMR5292,Lyon Neurosci Res Ctr,Brain Dynam &, Lyon, France
[27] Hosp Civils Lyon, Hop Edouard Herriot, Serv Audiol & Exporat Orofaciales, Lyon, France
[28] Klin Kinder & Jugendliche, Augsburg, Germany
[29] Univ Amsterdam, Acad Med Ctr, Dept Pediat Neurol, NL-1105 AZ Amsterdam, Netherlands
[30] Childrens Mem Hlth Inst, Dept Metab Dis, Warsaw, Poland
[31] Polish Acad Sci, Mossakowski Med Res Ctr, Dept Expt & Clin Neuropathol, Warsaw, Poland
[32] Univ Childrens Hosp Zurich, Div Clin Chem & Biochem, Zurich, Switzerland
[33] Zurich Ctr Integrat Human Physiol, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
DOPA-RESPONSIVE HYPERSOMNIA; DYSTONIA; GENE; HYPERPHENYLALANINEMIA; DISORDERS; MUTATIONS; SIBLINGS; PATIENT; REGION;
D O I
10.1002/ana.22685
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Sepiapterin reductase deficiency (SRD) is an under-recognized levodopa-responsive disorder. We describe clinical, biochemical, and molecular findings in a cohort of patients with this treatable condition. We aim to improve awareness of the phenotype and available diagnostic and therapeutic strategies to reduce delayed diagnosis or misdiagnosis, optimize management, and improve understanding of pathophysiologic mechanisms. Methods: Forty-three individuals with SRD were identified from 23 international medical centers. The phenotype and treatment response were assessed by chart review using a detailed standardized instrument and by literature review for cases for which records were unavailable. Results: In most cases, motor and language delays, axial hypotonia, dystonia, weakness, oculogyric crises, and diurnal fluctuation of symptoms with sleep benefit become evident in infancy or childhood. Average age of onset is 7 months, with delay to diagnosis of 9.1 years. Misdiagnoses of cerebral palsy (CP) are common. Most patients benefit dramatically from levodopa/carbidopa, often with further improvement with the addition of 5-hydroxytryptophan. Cerebrospinal fluid findings are distinctive. Diagnosis is confirmed by mutation analysis and/or enzyme activity measurement in cultured fibroblasts. Interpretation: Common, clinical findings of SRD, aside from oculogyric crises and diurnal fluctuation, are nonspecific and mimic CP with hypotonia or dystonia. Patients usually improve dramatically with treatment. Consequently, we recommend consideration of SRD not only in patients with levodopa-responsive motor disorders, but also in patients with developmental delays with axial hypotonia, and patients with unexplained or atypical presumed CP. Biochemical investigation of cerebrospinal fluid is the preferred method of initial investigation. Early diagnosis and treatment are recommended to prevent ongoing brain dysfunction. ANN NEUROL 2012; 71: 520-530
引用
收藏
页码:520 / 530
页数:11
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