- 同
- NALD
- 同
- NALD
WordNet
- relating to or affecting the infant during the first month after birth; "neonatal care"; "the neonatal period"
PrepTutorEJDIC
- 新生児の
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/08/09 10:35:07」(JST)
[Wiki en表示]
For the X-linked, juvenile or adult-onset condition, see Adrenoleukodystrophy.
| Neonatal adrenoleukodystrophy |
| Classification and external resources |
| OMIM |
202370 |
Neonatal adrenoleukodystrophy is an inborn error of peroxisome biogenesis. It is part of the Zellweger spectrum. It has been linked with multiple genes (at least five) associated with peroxisome biogenesis, and has an autosomal recessive pattern of inheritance.[1]
References
- ^ "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.
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Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders (E80.3, 277.86)
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| Peroxisome biogenesis disorder |
- Zellweger syndrome
- Neonatal adrenoleukodystrophy
- Infantile Refsum disease
- Adult Refsum disease-2
- RCP 1
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| Enzyme-related |
- Acatalasia
- RCP 2&3
- Mevalonate kinase deficiency
- D-bifunctional protein deficiency
- Adult Refsum disease-1
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| Transporter-related |
- X-linked adrenoleukodystrophy
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| Lysosomal |
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See also: proteins, intermediates
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Index of cells
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| Description |
- Structure
- Organelles
- peroxisome
- cytoskeleton
- centrosome
- epithelia
- cilia
- mitochondria
- Membranes
- Membrane transport
- ion channels
- vesicular transport
- solute carrier
- ABC transporters
- ATPase
- oxidoreduction-driven
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| Disease |
- Structural
- peroxisome
- cytoskeleton
- cilia
- mitochondria
- nucleus
- scleroprotein
- Membrane
- channelopathy
- solute carrier
- ATPase
- ABC transporters
- other
- extracellular ligands
- cell surface receptors
- intracellular signalling
- Vesicular transport
- Pore-forming toxins
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UpToDate Contents
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Japanese Journal
- Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans
- IMAMURA Atsushi,SHIMOZAWA Nobuyuki,SUZUKI Yasuyuki,ZHANG Zhongyi,TSUKAMOTO Toshiro,FUJIKI Yukio,ORII Tadao,OSUMI Takashi,KONDO Naomi
- Brain & development 22(1), 8-12, 2000-01-01
- NAID 10010096100
- 新生児型副腎白質ジストロフィーの1例 : ドコサヘキサエン酸(DHA)補充療法と臨床経過について
- 鈴木 康之,下沢 伸行,福田 ゆう子,市橋 寛,今村 淳,近藤 直実,折居 忠夫
- 日本先天代謝異常学会雑誌 11(2), 131, 1995-10-05
- NAID 10018923122
Related Links
- 20 Jun 2012 ... The neonatal adrenoleukodystrophy (NALD) page provides a brief description of the genetics and clinical features of this peroxisome biogenesis disorder (PBD) that is due to defects in either the PEX1, PEX5, PEX10, PEX13 ...
- Neonatal adrenoleukodystrophy is an inborn error of peroxisome biogenesis. It is part of the Zellweger spectrum. It has been linked with multiple genes (at least five) associated with peroxisome biogenesis, and has an autosomal recessive ...
★リンクテーブル★
[★]
- 英
- neonatal adrenoleukodystrophy
- 関
- ペルオキシソーム病、高ピペコリン酸血症、多発性ペルオキシソーム障害
[★]
多発性ペルオキシソーム障害
- 関
- hyperpipecolic acidemia、neonatal adrenoleukodystrophy、peroxisomal disorder
[★]
ペルオキシソーム病
- 関
- hyperpipecolic acidemia、multiple peroxisomal dysfunction、neonatal adrenoleukodystrophy
[★]
高ピペコリン酸血症
- 関
- multiple peroxisomal dysfunction、neonatal adrenoleukodystrophy、peroxisomal disorder
[★]
- 同
- neonatal adrenoleukodystrophy
[★]
- 関
- neonatal period、neonatally、neonate、newborn、newborn animal、newborn infant
[★]
副腎白質ジストロフィー ALD