WordNet

the 15th letter of the Roman alphabet (同)o
the blood group whose red cells carry neither the A nor B antigens; "people with type O blood are universal donors" (同)type_O, group O
abnormal development (of organs or cells) or an abnormal structure resulting from such growth

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1. 先天性股関節脱臼：治療および転帰 developmental dysplasia of the hip treatment and outcome
2. バレット食道のマネージメント management of barretts esophagus
3. 致死的骨格形成異常の出生前診断 prenatal diagnosis of the lethal skeletal dysplasias
4. 先天性股関節脱臼：臨床的特徴および診断 developmental dysplasia of the hip clinical features and diagnosis
5. 遺伝性皮膚症 the genodermatoses

[Median congenital fistula of the upper lip associated with Goldenhar syndrome: Report of a case].

Baptista C1, Bertrand B2, Bardot J3, Casanova D4, Degardin N5.
Annales de chirurgie plastique et esthetique.Ann Chir Plast Esthet.2015 May 22. pii: S0294-1260(15)00067-9. doi: 10.1016/j.anplas.2015.04.008. [Epub ahead of print]
AIM OF THE STUDY: We present the case of a patient with Goldenhar syndrome associated with congenital fistula in the middle of philtrum at the upper lip.PATIENTS AND METHODS: The patient was supported from birth for Goldenhar syndrome. Several procedures were performed in childhood to correct a macr
PMID 26006304

[Anesthetic management for surgery of esophagus atresia in a newborn with Goldenhar's syndrome].

Guerrero-Domínguez R1, López-Herrera-Rodríguez D2, Benítez-Linero I2, Ontanilla A3.
Revista brasileira de anestesiologia.Rev Bras Anestesiol.2015 May 7. pii: S0034-7094(13)00111-6. doi: 10.1016/j.bjan.2013.07.011. [Epub ahead of print]
BACKGROUND AND OBJECTIVES: Goldenhar's syndrome is a polymalformative condition consisting of a craniofacial dysostosis that determines difficult airway in up to 40% of cases. We described a case of a newborn with Goldenhar's syndrome with esophageal atresia and tracheoesophageal fistula who underwe
PMID 25960363

The incidence, embryology, and oculofacial abnormalities associated with eyelid colobomas.

Smith HB1, Verity DH1, Collin JR1.
Eye (London, England).Eye (Lond).2015 Apr;29(4):492-8. doi: 10.1038/eye.2014.335. Epub 2015 Jan 23.
PurposeTo describe a cohort of patients with congenital eyelid coloboma, to identify associated ocular and craniofacial abnormalities, and to establish any correlation between the size and location of eyelid colobomas and the presence of such abnormalities.MethodsAn observational case series of 55 p
PMID 25613848