パリスター・キリアン症候群。キリアン症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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English Journal
- The genetics of common disorders - Congenital diaphragmatic hernia.
- Slavotinek AM.
- European journal of medical genetics.Eur J Med Genet.2014 Aug;57(8):418-23. doi: 10.1016/j.ejmg.2014.04.012. Epub 2014 May 2.
- Congenital diaphragmatic hernia (CDH) is a common birth defect with a high mortality and morbidity. Although numerous chromosomal aberrations and gene mutations have been associated with CDH, the etiology of the diaphragmatic defect is identified in less than 50% of patients. This review discusses t
- PMID 24793812
- 12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome.
- Izumi K1, Zhang Z, Kaur M, Krantz ID.
- Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology.Chromosome Res.2014 Jul 1. [Epub ahead of print]
- Pallister-Killian syndrome is a multisystem sporadic genetic diagnosis characterized by facial dysmorphia, variable developmental delay and intellectual impairment, hypotonia, seizures, diaphragmatic hernia, and other systemic abnormalities. Pallister-Killian syndrome is typically caused by the pres
- PMID 24981202
- Cardiac manifestations of Pallister-Killian syndrome.
- Tilton RK1, Wilkens A, Krantz ID, Izumi K.
- American journal of medical genetics. Part A.Am J Med Genet A.2014 May;164A(5):1130-5. doi: 10.1002/ajmg.a.36413. Epub 2014 Feb 6.
- Pallister-Killian syndrome (PKS) is a sporadic multisystem genetic diagnosis characterized by facial dysmorphia, variable developmental delay and intellectual impairment, hypotonia, hearing loss, seizures, differences in skin pigmentation, temporal alopecia, diaphragmatic hernia, congenital heart de
- PMID 24504854
Japanese Journal
- Amniocentesis can be useful during the third trimester of pregnancy for antenatal diagnosis of Pallister-Killian syndrome: a case report
- Murakami M.,Iwasa T.,Takahashi Y.,Morine M.
- CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY 38(3), 269-271, 2011
- NAID 120005207093
- Brain MRI findings of older patients with Pallister-Killian syndrome
- SAITO Yoshiaki,MASUKO Kaori,KANEKO Kaori,CHIKUMARU Yuri,SAITO Kazuyo,IWAMOTO Hiroko,MATSUI Akira,AIDA Noriko,KUROSAWA Kenji,KUROKI Yoshikazu,KIMURA Seiji
- Brain & development 28(1), 34-38, 2006-01
- NAID 10017319196
- <原著論文>羊水細胞を用いた染色体異常の出生前診断 : 秋田県において10年間に行った535例の解析
Related Links
- Pallister-Killian syndrome (also tetrasomy 12p mosaicism or Pallister mosaic aneuploidy syndrome) is an extremely rare genetic disorder occurring in humans. Pallister-Killian occurs due to the presence of the anomalous extra isochromosome ...
- Pallister-Killian mosaic syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by extremely weak muscle tone (hypotonia) in infancy and early childhood, intellectual ...
★リンクテーブル★
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- 英
- Pallister-Killian syndrome
- 同
- パリスター症候群 Pallister syndrome、キリアン症候群 Killian syndrome、パリスター-キリアン症候群
参考
- http://www.pk-syndrome.org/pks_desc_e.htm
- http://www.pkskids.net/UNIQUE.pdf
- http://en.wikipedia.org/wiki/Pallister%E2%80%93Killian_syndrome
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パリスター・キリアン症候群
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