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.com

Volume 4

Neonatal and Pediatric Medicine

Pediatrics Neonatal Care 2018

November 12-13, 2018

November 12-13, 2018 Dubai, UAE

22

nd

World Congress on

Pediatrics, Neonatology & Primary Care

Recent advances in understanding the pathophysiology and management of cystic fibrosis

Abeer Mohi El-Din Saleh

International Medical Center Hospital, Egypt

A

lthough cystic fibrosis is a monogenic, predominantly Caucasian, autosomal recessive disease, increasing numbers of

patients with cystic fibrosis are being identified in other large populations. It was first recognized as a specific disease by

Dorothy Andersen in 1938, with descriptions that fit the condition occurring at least as far back as 1595. The cystic fibrosis

trans membrane conductance regulator gene was identified in 1989. It affects multiple organs, including the intestine, sweat

glands, pancreas and the reproductive system, but cystic fibrosis lung disease causes most morbidity and leads to premature

mortality. It’s now predicted that children born with cystic fibrosis in the 2000s will survive into their 50s. The focus of this review

is to summarize some of the recent advances that have taken place in our understanding of the recent advances in diagnosing and

managing cystic fibrosis.

Biography

Abeer Mohi El-Din Saleh has completed Bachelor’s degree from Ain Shams University Faculty of Medicine in 1995, Master’s degree from the same university in

2001 and MRCPCH London, UK in 2013. She has previously worked in Yeovil District Hospital, UK. She is currently is working as a Pediatric Consultant in the

International Medical Center Hospital and Nasser Institute, Cairo, Egypt.

Abeer Mohi El-Din Saleh, Neonat Pediatr Med 2018, Volume 4

DOI: 10.4172/2572-4983-C3-008