WordNet
- the quality of being dolichocephalic (同)dolichocephalism
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/12/31 22:17:32」(JST)
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- 1. 頭蓋骨縫合早期癒合症の概要 overview of craniosynostosis
- 2. 妊娠期間および出産予定日の出生前評価 prenatal assessment of gestational age and estimated date of delivery
- 3. 幼児および小児における巨頭症：病因および評価 macrocephaly in infants and children etiology and evaluation
- 4. 先天性ミオパシー congenital myopathies
- 5. 幼児および小児における精密な神経学的評価 detailed neurologic assessment of infants and children
English Journal
- Individual course of cranial symmetry and proportion in preterm infants up to 6 months of corrected age.
- Ifflaender S1, Rüdiger M2, Konstantelos D1, Lange U1, Burkhardt W1.
- Early human development.Early Hum Dev.2014 Sep;90(9):511-5. doi: 10.1016/j.earlhumdev.2014.03.008. Epub 2014 Apr 21.
- INTRODUCTION: A significant proportion of preterm infants have dolichocephaly and/or deformational plagiocephaly (DP) at term equivalent age. However, quantitative data on the clinical course after discharge is limited in these infants.AIMS: To quantify the individual course of cranial symmetry and
- PMID 24751496
- Neonatal Marfan syndrome: a successful early multidisciplinary approach.
- Amado M1, Calado MA1, Ferreira R2, Lourenço T3.
- BMJ case reports.BMJ Case Rep.2014 Jun 13;2014. pii: bcr2013202438. doi: 10.1136/bcr-2013-202438.
- Marfan syndrome (MFS) is a genetic disorder of the connective tissue which rarely manifests in the neonatal period and has an ominous prognosis. A case of a first female offspring of healthy parents is described here. The pregnancy was uneventful and the mother had a term caesarean delivery. At birt
- PMID 24928929
- A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5.
- Krgovic D, Blatnik A, Burmas A, Zagorac A, Kokalj Vokac N1.
- BMC medical genetics.BMC Med Genet.2014 Feb 11;15:21. doi: 10.1186/1471-2350-15-21.
- BACKGROUND: Rearrangements involving chromosome 5p often result in two syndromes, Cri-du-chat (CdC) and Trisomy 5p, caused by a deletion and duplication, respectively. The 5p15.2 has been defined as a critical region for CdC syndrome; however, genotype-phenotype studies allowed isolation of particul
- PMID 24517234
Japanese Journal
- Metric traits of the crania and limb bones of medieval human skeletons from Kamakura City, Japan
- Anthropological Science 123(1), 41-55, 2015
- NAID 130005066008
- Metric traits of the crania and limb bones of medieval human skeletons from Kamakura City, Japan
- Anthropological Science advpub(0), 2015
- NAID 130004832144
- A Case of Sotos Syndrome Treated with Distraction Osteogenesis in Maxilla and Mandible
- The Bulletin of Tokyo Dental College 53(2), 75-82, 2012
- NAID 130004471722
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