Nilgün Köksal

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Sacrococcygeal teratoma (SCT) is rarely associated with syndromes. We report a female newborn with a prenatal diagnosis of small sacrococcygeal teratoma and postnatally diagnosed as having trisomy 13. The sacrococcygeal teratoma was excised. It was reported as mature teratoma. The child succumbed to sepsis postoperatively.
  • OLGU BİLDİRİMİ, Joubert Sendromu, +7 authors V. Saraç
  • 2004
Anahtar Kelimeler: Joubert sendromu. Molar diş görünümü. Vermis hipoplazi. Epizodik hiperpne. ABSTRACT Joubert syndrome is a rare autosomol recessive disorder whose main clinical signs are hypotonia, ataxia, mental retardation, abnormal eye movements and a respiratory pattern of alternating tachypnea-apnea.The most characteristic imaging features are(More)
Gastro-esophageal reflux (GER) is one of the common problems of neonatal intensive care units. Although this condition does not always need to be treated, it occasionally causes clinically serious consequences. Initial management is medical; however, in some cases surgery might be required. A premature neonate with birth weight of 1370 grams was managed in(More)
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