Literature DB >> 18500735

Doll-like face: is it an underestimated clinical presentation of cystic fibrosis?

Mehmet Kose1, Sevgi Pekcan, Nural Kiper, Ayse Tana Aslan, Nazan Cobanoglu, Ebru Yalcin, Deniz Dogru, Ugur Ozcelik.   

Abstract

UNLABELLED: Cystic fibrosis (CF) is the most prevalant inheritable chronic disease in caucasian children. The clinical syndrome of kwashiorkor is well-recognized complication of CF. The edema of the face can be seen in kwashiorkor. As doll-like face is very rare and underestimated clinical presentation of CF patients complicated with hypoproteinemia we evaluated demographic features and laboratory characteristics of 5 patients diagnosed as CF with doll-like face.
METHODS: Between June 2005 and January 2008, 115 children were diagnosed as having CF enrolled in our center. Five infants were diagnosed as CF with doll-like face before the age of 6 months participitated in study.
RESULTS: The incidence of doll-like face younger than the 6 months of age were 9.4% in our center. 48 infants diagnosed as CF without doll-like face before the age of 6 months participitated in the study as controls (group2). Physical examination revealed doll-like face and pitting edema of lower extremities in group 1. Their weight and length were under the third centile. Laboratory findings of group 1 include: mean hemoglobin 7.6g/dl; mean total protein 4.4 g/dl; albumin 2.3 g/dl. When compared control group in order to; 11.4 g/dl (range 7.6-17.9); 6.2 g/dl (range 4.0-8.8); 4.7 g/dl (range 2.1-5.8). mean hemoglobin, total protein and albumin values were lower in group 1.
CONCLUSION: In a subgroup of patients, doll-like face may be the presenting manifestation of CF. Especially in developing countries clinicians should be aware of in patients with malnutrition and doll-like face and CF should be considered in differential diagnosis.

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Year:  2008        PMID: 18500735     DOI: 10.1002/ppul.20819

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  3 in total

1.  Early severe anemia as the first sign of cystic fibrosis.

Authors:  Tugba Sismanlar; Ayşe Tana Aslan; Mehmet Köse; Sevgi Pekcan; Fatih Süheyl Ezgü; Işıl İrem Budakoğlu; İdil Yenicesu
Journal:  Eur J Pediatr       Date:  2016-08-05       Impact factor: 3.183

2.  The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.

Authors:  Murat Erdoğan; Mehmet Köse; Sevgi Pekcan; Melih Hangül; Burhan Balta; Aslıhan Kiraz; Gizem Akıncı Gönen; Ayşe Gül Zamani; Mahmut Selam Yıldırım; Tuğba Ramaslı Gürsoy; Fatih Ezgu; Tuğba Şişmanlar Eyüpoğlu; Ayse Tana Aslan
Journal:  Balkan Med J       Date:  2021-11       Impact factor: 2.021

3.  The Incidence of Cystic Fibrosis in the Central Region of Anatolia in Turkey Between 2015 and 2016

Authors:  Melih Hangül; Sevgi Pekcan; Mehmet Köse; Deniz Acıcan; Tuba Esra Şahlar; Murat Erdoğan; Mustafa Kendirci; Deniz Güney; Hasan Öznavruz; Osman Demir; Ömür Ercan; Fatma Göçlü
Journal:  Balkan Med J       Date:  2018-12-28       Impact factor: 2.021

  3 in total

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