Harlequin colour change in a neonate with perinatal asphyxia: An unusual pattern

Mithlesh Dewangan

Ectrodadactyly

Sindhu MARU, Thumjaa ANNAMALAİ, Raja Selvan RAJENDRAN, Vamsi Krishna REDDY K

Incontinentia Pigmenti in a newborn: Case report and review of the literature

Margarida Silva Fonseca, Maria do Céu Ribeiro, Sónia Lira, Alberto Mota

Role of post-operative radiation therapy in single brain metastasis from clear cell sarcoma in children: a case report with systemic review

Fadoua RAİS, Naoual BENHMİDOU, Ghizlane RAİS, Hasnaa LOUGHLİMİ, Maghous ABDELHAK, Khadija BELLAHAMMOU, Fadila KOUHEN, Jihan AARAB, Sanaa ELMEJJAOUİ, Tayeb KEBDANİ, Hanan ELKACEMİ, Noureddine BENJAAFAR

Rupture of sinus of valsalva aneurysm: earliest presentation in association with ventricular septal defect and aortic regurgitation

Binoy SHANKAR, Sanjay KUMAR, Dinesh KUMAR

Gastrointestinal trichobezoar causing atypical intussusception in a child: report of two cases

Rachida LAAMİRİ, Nahla KECHİCHE, Walid MNARİ, Habib BESBES, Samia BELHASSEN, Sana MOSBAHİ, Amine KSİA, Lassaad Sahnoun, Mongi Mekki, Mohsen Belghith, Abdellatif Nouri

Effect of vitamin D supplementation on growth parameters in children with vitamin D deficiency

Yashwant RAO, Tanu MİDHA, Prashant TRİPATHİ, Satyajeet SİNGH, Rahul Deo SHARMA, Sunisha ARORA

New Generation Surfactants, Are They A Hope For Better Outcomes?

Seçil Erçin, Fahri Ovali

The effect of intestinal microbiome on autism spectrum disorder

Maria Gogou, Christiana Gogou

Buccal Cellulitis in 3 Infants

Martin Stallings

Subclinical left ventricle dysfunction revealed by echocardiography in a neonate with a neck hemangioma

Maria GOGOU, Anastasia KEİVANİDOU, Andreas GİANNOPOULOS

A Rare Case of Conjoined Twin: Deradelphus with Review of Existing Literature

Mithun Konar, Kriti Rana, Kanai Barik

Scurvy – Still an added co-morbidity in Children with Cerebral Palsy

Mithun Konar, Kriti Rana, Manoj Maiti, Kanai Barik

Magnetic Resonance Spectroscopy for the Diagnosis of Unusual Case of Cystecercal Meningoencephalitis

Anita Kumari, Gaurav Mukhija, Ajeet Singh

Paternally inherited 17q12 microduplication: similar pattern of neurological signs and features in the father and his children

Piero Pavone, Andrea Domenico Praticò, Raffaele Falsaperla, Nicola Beltrami, Alberto Verrotti, Martino Ruggieri

Spontaneous rupture of congenital hydrocephalous: a rare complication

Anuj Dhyani, Suresh Goyal

Hallervorden spatz syndrome: a case report

Poonam MEHTA, Anjali SİNGH, Geeta GATHWALA, Seema ROHİLLA

Megalencephalic leukoencephalopathy with temporal cysts

Nabanita KORA, Kaustav NAYEK

Inverse Marcus Gunn phenomenon

Alexandra Fernandes, Mariana Abreu, Sofia Fernandes, Inês Maio, Fátima Pinto