The Effect of Nutritional Counseling via Printed Recipe Cards Versus Verbal on Growth of a Cohort of Egyptian Children with Cystic Fibrosis

2022 ◽  
Vol 2 (1) ◽  
pp. 17-24
Author(s):  
Dina Hamed ◽  
Hala Hamdi ◽  
Aya Saeed ◽  
Shrouk Moataz Abdallah
2020 ◽  
Vol 1 (1) ◽  
pp. 1-6
Author(s):  
Mona El Falaki ◽  
Mona El Attar ◽  
Nossa El Basha ◽  
Nihal El Refai ◽  
Walaa Shahin ◽  
...  

2006 ◽  
Vol 5 ◽  
pp. S103
Author(s):  
M.L. Naguib ◽  
I. Schrijver ◽  
P. Gardner ◽  
L.M. Piquet ◽  
S.S. Doss ◽  
...  

2020 ◽  
Vol 09 (03) ◽  
pp. 164-170
Author(s):  
Mohammad Al-Haggar ◽  
Engy Osman ◽  
Abdel-Rahman Eid ◽  
Tarek Barakat ◽  
Samar El-Morsi

AbstractCystic fibrosis (CF) is panethnic autosomal recessive disease that affects the exocrine glands of pancreas, lungs, and intestine. It is often misdiagnosed in developing countries as difficult-to-treat asthma. We enrolled 150 Egyptian families with one or more probands who were complaining of difficult-to-treat asthma, and 112 cases were studied extensively through history taking including pedigree construction and clinical examination. In addition, spirometry and computed tomography of the chest were done in selected cases. All cases were subjected to quantitative sweat chloride test and molecular screening for the three most common mutations of cystic fibrosis transconductance regulator (CFTR) gene (ΔF508, G542X, W1282X) using amplification refractory mutation system (ARMS) technique. Probands of difficult-to-treat asthma comprised 66 males and 46 females; their age range was 1 to 14 years. Sixty-one probands (54.5%) were carriers of one or more of the studied mutations (36 cases and 25 carriers). Six carriers of single mutations had mild respiratory symptoms and negative sweat test. The most common allele was ΔF508, 60 alleles in 56 individuals (4 were homozygous ΔF508/ΔF508) followed by W1282X in 25 individuals and G542X in 12 individuals. Allele W1282X had an increased risk of recurrent chest infection and bronchiectasis. Moreover, cases with two mutations had more severe symptoms compared with those with a single mutation. CFTR mutations and CF-related syndromes are not rare as thought in Egypt, especially among the high-risk difficult-to-treat asthma. The readily available ARMS technique is recommended for ΔF508 and/or W1282X screening on priority basis among these children.


2007 ◽  
Vol 6 (2) ◽  
pp. 111-116 ◽  
Author(s):  
Maggie L. Naguib ◽  
Iris Schrijver ◽  
Phyllis Gardner ◽  
Lynn M. Pique ◽  
Samiha S. Doss ◽  
...  

2017 ◽  
Vol 65 (1) ◽  
pp. 21-24
Author(s):  
Mona Mohsen El Attar ◽  
Noha Musa Azab ◽  
Dina Hossam El Dine Hamed ◽  
Ahmed Shawky Abdelbasir Tawfik

2016 ◽  
Vol 10 (2) ◽  
pp. 197
Author(s):  
HalaM Koura ◽  
MaggieL Naguib ◽  
MonaM Mahmoud ◽  
AtefS Mohamed ◽  
SamihaS Wissa

SpringerPlus ◽  
2016 ◽  
Vol 5 (1) ◽  
Author(s):  
Walaa Aboulkasem Shahin ◽  
Dina Ahmed Mehaney ◽  
Mona Mostafa El-Falaki

JAMA ◽  
1966 ◽  
Vol 195 (12) ◽  
pp. 993-1000 ◽  
Author(s):  
R. J. Grand
Keyword(s):  

Author(s):  
J. V. Briggman ◽  
J. Bigelow ◽  
H. Bank ◽  
S. S. Spicer

The prevalence of strands shown by freeze-fracture in the zonula occludens of junctional complexes is thought to correspond closely with the transepi-thelial electrical resistance and with the tightness of the junction and its obstruction to paracellular flow.1 The complexity of the network of junc¬tional complex strands does not appear invariably related to the degree of tightness of the junction, however, as rabbit ileal junctions have a complex network of strands and are permeable to lanthanum. In human eccrine sweat glands the extent of paracellular relative to transcellular flow remains unknown, both for secretion of the isotonic precursor fluid by the coil and for resorption of a hypertonic solution by the duct. The studies reported here undertook, therefore, to determine with the freeze-fracture technique the complexity of the network of ridges in the junctional complexes between cells in the secretory coil and the sweat ducts. Glands from a patient with cystic fibrosis were also examined because an alteration in junctional strands could underlie the decreased Na+ resorption by sweat ducts in this disease. Freeze-fracture replicas were prepared by standard procedures on isolated coil and duct segments of human sweat glands. Junctional complexes between clear cells, between dark cells and between clear and dark cells on the main lumen, and between clear cells on intercellular canaliculi of the coil con¬tained abundant anastomosing closely spaced strands averaging 6.4 + 0.7 (mean + SE) and 9.0 +0.5 (Fig. 1) per complex, respectively. Thus, the junctions in the intercellular canaliculi of the coil appeared comparable in complexity to those of tight epithlia. Occasional junctions exhibited, in addition, 2 to 5 widely spaced anastomosing strands in a very close network basal to the compact network. The fewer junctional complexes observed thus far between the superficial duct cells consisted on the average of 6 strands arranged in a close network and 1 to 4 underlying strands that lay widely separated from one another (Fig. 2). The duct epitelium would, thus, be judged slightly more "leaky" than the coil. Infrequent junctional complexes observed to date in the secretory coil segment of a cystic fibrosis specimen disclosed rela¬tively few closely crowded strands.


1999 ◽  
Vol 37 (4) ◽  
pp. 291-293 ◽  
Author(s):  
B. Cimon ◽  
J. Carrere ◽  
J. P. Chazalette ◽  
J. F. Vinatier ◽  
D. Chabasse ◽  
...  

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