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1. ファブリー病の臨床的特徴および診断 clinical features and diagnosis of fabry disease
2. 異染性白質ジストロフィー metachromatic leukodystrophy
3. 小児における後天性末梢性ニューロパチーの概要 overview of acquired peripheral neuropathies in children
4. 遺伝性感覚自律神経ニューロパチー hereditary sensory and autonomic neuropathies
5. 大顆粒T細胞リンパ球性白血病の臨床症状、病理学的特徴、および診断 clinical manifestations pathologic features and diagnosis of t cell large granular lymphocyte leukemia

Japanese Journal

課題】皮膚中でのセラミドの炭酸水とビタミンCを用いた顔分化するが、セミノリピドサルファタイドは、神経組織のなどのスフィンゴリピド：N−アシルスフィン MC-5とスフィンゴミエリン異染性白質ジストロフィー症

リンク元	「リピドーシス」
拡張検索	「スフィンゴリピドーシス」「リゾスフィンゴリピド」「スフィンゴリピド症」

Disease	Enzyme Deficiency	Lipid Accumulating	Clinical Symptoms
Tay-Sachs disease	Hexosaminidase A	Cer-Glc-Gal(NeuAc)-: : GalNAc GM2 Ganglioside	Mental retardation, blindness, muscular weakness.
Fabry's disease	α-Galactosidase	Cer-Glc-Gal-: : Gal Globotriaosylceramide	Skin rash, kidney failure (full symptoms only in males; X-linked recessive).
Metachromatic leukodystrophy	Arylsulfatase A	Cer-Gal-: : OSO3 3-Sulfogalactosylceramide	Mental retardation and psychologic disturbances in adults; demyelination.
Krabbe's disease	β-Galactosidase	Cer-: : Gal Galactosylceramide	Mental retardation; myelin almost absent.
Gaucher's disease	β-Glucosidase	Cer-: : Glc Glucosylceramide	Enlarged liver and spleen, erosion of long bones, mental retardation in infants.
Niemann-Pick disease	Sphingomyelinase	Cer-: : P-choline Sphingomyelin	Enlarged liver and spleen, mental retardation; fatal in early life.
Farber's disease	Ceramidase	Acyl-: : Sphingosine Ceramide	Hoarseness, dermatitis, skeletal deformation, mental retardation; fatal in early life.