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- Primary progressive MS resembles tropical spastic paraplegia, a known STD. 最初的進(jìn)展性MS類(lèi)似局部痙攣性麻痹，一種已知的STD。
- ERDA1 gene and SEF2-1 gene nucleotide repeated sequence in patients with hereditary spastic paraplegia. 遺傳性痙攣性截癱患者ERDA1和SEF2-1基因三核苷酸重復序列的研究
- The gene defect accounts for 6 percent to 7 percent of all cases of hereditary spastic paraplegia, they said. 6-7%25的遺傳性痙攣性截癱患者存在該基因缺陷。
- Objective To investigate the clinical and genetic characteristics of hereditary spastic paraplegia(HSP). 目的探討遺傳性痙攣性截癱的臨床和遺傳特點(diǎn)。
- The Duke scientists began their search for genes associated with the disease by studying two families whose members had hereditary spastic paraplegia. 杜克研究中心的科學(xué)家們研究了兩個(gè)存在遺傳性痙攣性截癱患者的家庭。
- Laurence-Moon syndrome is a rare hereditary condition associated with retinitis pigmentosa, spastic paraplegia, hypogonadism and mental retardation. 什么是'勞倫斯文綜合征-遺傳綜合征與精神發(fā)育遲滯和性腺機能減退'?
- Aim: To explore the feature of hereditary spastic paraplegia with thin corpus callosum ( HSP-TCC) for the profound recognition of this disease. 目的:分析遺傳性痙攣性截癱伴胼胝體發(fā)育不良(HSP-TCC)的臨床特點(diǎn),以提高對此病的認識。
- In their study, the Duke researchers found that one form of hereditary spastic paraplegia is linked to a gene called REEP1. 杜克的研究人員發(fā)現其中一種遺傳性痙攣性截癱與REEP1基因有關(guān)。
- Hereditary spastic paraplegia, one of a number of related inherited disorders, causes progressive limb weakness and stiffness, often resulting in paralysis. 遺傳性痙攣性截癱是一種遺傳性疾病，患者癥狀是下肢進(jìn)行性萎縮和僵直，其中大多最終將癱瘓。
- DURHAM, N.C.-- Scientists have linked a recently discovered gene to a rare nervous system disease called hereditary spastic paraplegia, for which there is no cure. 科學(xué)家最近發(fā)現一種新的基因可能與罕見(jiàn)的神經(jīng)系統疾病--遺傳性痙攣性截癱有關(guān)，該疾病目前尚無(wú)有效的治療方法。
- Results: All the 30 HM patients(100%) had typical clinical fealures of spastic paraplegia(SP) but without sensory dysfunction.4 of 30 cases(13.3%)received portacaval shunt(PCS). 4例(13.;3%25)曾接受門(mén)腔靜脈分流術(shù);28例(93
- BackgroundHereditary spastic paraplegia (HSP or SPG) is a kind of hereditary disorder of nervous system. Autosomal dominant (AD), autosomal recessive (AR), X-linked inheritance have been described for HSP. 遺傳性痙攣性截癱(hereditary spastic paraplegia，HSP或SPG)是一種神經(jīng)系統遺傳病，呈常染色體顯性遺傳(autosomal dominant，AD)、常染色體隱性遺傳(autosomal recessive，AR)和X-連鎖隱性遺傳(X-linked recessive，XR)，其中以AD遺傳最為常見(jiàn)。
- Hereditary spastic paraplegias (HSP) are characterised by symmetric spastic paraplegia, pallhypaesthesia, and urinary dysfunction (uncomplicated HSP). 什麼是'遺傳性痙攣性截癱-繼承類(lèi)型的癱瘓'?
- Marfan rs disease progressive spastic paraplegia 進(jìn)行性痙攣性截癱
- hereditary spastic paraplegia(HSP) 遺傳性痙攣性截癱
- Familial spastic paraplegia syndrome 家族性痙攣性截癱綜合征
- Marfan's disease progressive spastic paraplegia 進(jìn)行性痙攣性截癱
- Tropical plants abound in the jungle. 叢林中有大量的熱帶植物。
- Athetosis with spastic paraplegia 手足徐動(dòng)癥伴痙攣性截癱
- These tropical flowers have bright colors. 這些熱帶花卉顏色很艷麗。
