Yusuf Kale
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Early neonatal outcomes of very-low-birth-weight infants in Turkey: A prospective multicenter study of the Turkish Neonatal Society Open
View article: Nasal Glioma in an Extremely Low Birth Infant: A Case Report
Nasal Glioma in an Extremely Low Birth Infant: A Case Report Open
Neuroglial heterotopias are rare congenital masses.Nasal heterotopies are termed as nasal glial heterotopia or nasal glioma.The differential diagnosis includes hemangioma, dermoid/epidermoid cysts, encephalocel and tumors.Surgical excision…
View article: Çok Düşük Doğum Ağırlıklı Bebekte Nazal Gliom: Olgu Sunumu
Çok Düşük Doğum Ağırlıklı Bebekte Nazal Gliom: Olgu Sunumu Open
Nöroglial heterotopiler nadir görülen konjenital kitlelerdir. Nazal heterotopiler nazal glial heterotopiveya nazal gliom olarak adlandırılır. Ayırıcı tanıda hemanjiom, dermoid / epidermoid kistler, ensefaloselve tümörler bulunmaktadır. Cer…
View article: Kraniyal görüntüleme bulguları ile akçaağaç şurubu idrar hastalığı
Kraniyal görüntüleme bulguları ile akçaağaç şurubu idrar hastalığı Open
Dallı-zincirli ketoasidüri olarak da bilinen Akçaağaç şurubu idrar hastalığı (MSUD) dallı-zincirli alfa ketoasit dehidrogenaz kompleks aktivitesindeki yetersizliğinden kaynaklanır. Otozomal resesif olarak kalıtılan bir hastalıktır. Yenidoğ…
View article: Congenital glaucoma accompanied by natal teeth: A case report
Congenital glaucoma accompanied by natal teeth: A case report Open
Primary congenital glaucoma is a global problem, which is characterized by increased intraocular pressure and resulted in loss of vision if not timely and appropriately treated. Natal teeth is a rare case which is characterized by the exis…
View article: Retinopathy of Prematurity in Triplets
Retinopathy of Prematurity in Triplets Open
ROP in triplets seems to be mainly related to low gestational age and low birth weight. Further prospective randomized studies are necessary to demonstrate risk factors of ROP in triplets and to determine if and how gemelarity plays a role…
View article: A case of zellweger syndrome accompanied by hypertrophic cardiomyopathy
A case of zellweger syndrome accompanied by hypertrophic cardiomyopathy Open
Peroxisomal biogenesis disorders are a group of genetically and clinically heterogenous disorders which affect very-long chain fatty acid metabolism. Zellweger syndrome (ZS) is a rare, congenital disorder characterized by multisystem invol…
View article: Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report
Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report Open
Chilaiditi syndrome is a variant of the rotation of the colon that gives rise to the interposition of the colon between the right diaphragm and the liver intermittently or constantly. Also, Necrotizing enterocolitis is typically seen in pr…
View article: Type VI Aplasia Cutis Congenita: Bart’s Syndrome
Type VI Aplasia Cutis Congenita: Bart’s Syndrome Open
Bart’s syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart’s…