5 results on '"M. De Keukelaere"'
Search Results
2. Activerende PI3Kδ-mutaties: klinische en biochemische presentatie van behandelbare primaire immuundeficiënties
- Author
-
I. Meyts, M. De Keukelaere, and C. Bucciol
- Subjects
0301 basic medicine ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,business.industry ,Medicine ,General Medicine ,business ,030215 immunology - Abstract
Activating PI3Kδ mutations: clinical and biochemical presentation of treatable primary immune deficiencies The field of primary immune deficiencies is expanding rapidly. Recently, gain-of-function (GOF) mutations in the phosphoinositide 3 kinase (PI3K) CD and PI3KR1 genes have been reported to cause a clinical syndrome referred to as activated PI3Kδ syndrome (APDS). APDS is characterized by severe bacterial and viral infections, upper and lower respiratory tract infections with bronchiectasis, severe herpes virus infections, lymphoproliferation and lymphoma formation, but the clinical phenotype can be highly variable. In this article 2 patients with APDS are presented with an emphasis on the clinical and immunological features that should alert a physician to the possibility of the diagnosis. It is important because targeted therapy can change the course of the disease.
- Published
- 2021
- Full Text
- View/download PDF
3. Nausea is the only symptom associated with delayed gastric emptying in pediatric functional dyspepsia patients.
- Author
-
De Keukelaere M, Carbone F, van Hoeve K, Tack J, and Hoffman I
- Subjects
- Female, Humans, Child, Adolescent, Male, Nausea diagnosis, Abdominal Pain diagnosis, Vomiting, Dyspepsia diagnosis, Gastroparesis
- Abstract
Objectives: Functional dyspepsia (FD) is a heterogeneous functional gastrointestinal disorder (FGID) with a highly prevalent symptom complex. The aim of our study is to investigate the relation between symptoms of FD and results of gastric emptying (GE) breath test in children., Methods: This study included patients (6-17 years old) presented at the general gastroenterology outpatient clinic with dyspeptic symptoms (Rome IV criteria) and underwent careful history taking with clinical examination. A GE breath test with a
13 C-octanoic acid labeled (250 kcal) solid meal was performed and dyspepsia symptom scores, clarified using pictograms for postprandial fullness, bloating, belching, nausea, vomiting, epigastric pain and burning, were obtained every 15 min ranging from 0 to 4 for a total of 240 min. The severity of the complaints (overall and individual symptoms) as displayed by the symptom questionnaire was compared between normal and delayed GE groups. The relationship between GE time and the severity of FD symptoms was assessed using Mann-Whitney test., Results: Thirty nine FD patients (55% girls; mean age: 11.9 ± 3.3 years) participated in the study. Of these, 43% had delayed GE. The overall symptom severity in patients with delayed GE was similar to the symptoms of patients with a normal GE rate (149.5 ± 12.7 points vs. 123.9 ± 9.0; p = 0.19). Individual symptoms scores showed only nausea to be significantly increased in the group with delayed GE (21.5 ± 1.9 points vs. 33.2 ± 4.6; p = 0.048, p < 0.1)., Conclusion: Especially in children with nausea as presenting symptom of FD, a low threshold should be withheld to perform a GE breath test., (© 2023 John Wiley & Sons Ltd.)- Published
- 2023
- Full Text
- View/download PDF
4. Child with protein losing enteropathy as presentation of collagenous duodenitis and eosinophilic gastroenteritis.
- Author
-
van Hoeve K, De Keukelaere M, De Hertogh G, and Hoffman I
- Subjects
- Serum Albumin, Child, Preschool, Proton Pump Inhibitors therapeutic use, Female, Humans, Eosinophilia, Histamine Antagonists administration & dosage, Enteritis, Duodenitis diagnosis, Duodenitis drug therapy, Edema etiology, Protein-Losing Enteropathies diagnosis, Gastritis diagnosis, Gastritis drug therapy, Diarrhea etiology
- Abstract
Background: Collagenous duodenitis and gastritis are rare histopathological findings in children., Patients and Methods: : We describe a four-year old girl, who presented with non-bloody diarrhea for two months and progressive edema with an albumin of 16g/dl., Results: The diagnosis of a protein losing enteropathy was made. Extensive investigations withheld only an infectious cause of the protein losing enteropathy (cytomegalovirus and adenovirus). However, the patients still required repetitive albumin infusions 3.5 months after onset of symptoms without spontaneous recovery. Therefore, a new endoscopic work-up was performed. Duodenal biopsies revealed collagen deposition, in association with a high number of eosinophils and mast cells throughout different parts of the gastrointestinal tract., Conclusions: The collagen deposition seems to be triggered by an eosinophilic gastrointestinal disorder. Treatment was started with amino acid-based formula, oral iron therapy, an antihistamine, and a proton pomp inhibitor that resulted in persistent normalization of serum albumin already after 1.5 weeks., Competing Interests: The authors declare that they have no conflict of interest, (© Acta Gastro-Enterologica Belgica.)
- Published
- 2023
- Full Text
- View/download PDF
5. Evolution of body mass index in children with type 1 diabetes mellitus.
- Author
-
De Keukelaere M, Fieuws S, Reynaert N, Vandoorne E, Kerckhove KV, Asscherickx W, and Casteels K
- Subjects
- Adolescent, Body Weight, Child, Child, Preschool, Female, Humans, Infant, Longitudinal Studies, Male, Pediatric Obesity epidemiology, Prevalence, Retrospective Studies, Time Factors, Body Mass Index, Diabetes Mellitus, Type 1 complications, Pediatric Obesity etiology
- Abstract
The prevalence of childhood overweight and obesity has risen during the last 30 years, not only in children with type 2 diabetes, but also those with type 1 (T1D) and this is linked with an increased cardiovascular risk. A better understanding of weight patterns in the years after diagnosis of T1D is important to identify those children with a risk for excess weight gain and strategies to decrease this. We retrospectively analyzed data of all children with T1D followed at the department of Pediatric Endocrinology Leuven and diagnosed between 1991 and 2015. Data as age, sex, BMI, and Tanner score were extracted in 390 subjects. Standardized BMI (BMI SDS) in this study group using all data was 0.26. An increase in BMI SDS was seen as a function of time since diagnosis and age, both being independent predictors. Data comparison showed a significant stronger relation between BMI SDS and both time since diagnosis and age in girls. Children diagnosed after puberty showed a higher increase in BMI SDS.Conclusion: These longitudinal data suggest an important increase in BMI in children with T1D, both as a function of time since diagnosis and age, especially in girls. What is Known: • The prevalence of childhood overweight and obesity is risen during the last 30 years, in children with type 2 diabetes, but also those with type 1 diabetes. What is New: • Our study demonstrates with longitudinal data an increase in BMI in children with type 1 diabetes, especially girls. The increase in BMI SDS is seen as a function of time since diagnosis and age, both being independent predictors. Given the increased risk of metabolic syndrome and other complications in overweight children, special attention is needed to prevent this evolution.
- Published
- 2018
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.