Back to program Thursday Back to program Friday

Thursday 16 March - Posterwalk 1 (PW 1 - PW 10)
10:30 - 11:00 
PW 1

Group A Streptococcus meningitis: report of a case
Jules Lagrou, HUDERF

PW 2

Pleural empyema at 1 month of age: important considerations and pitfalls, a case report
Sari Daelemans, UZ Brussel

PW 3

Ivana Lion, U Liège

PW 5

Immune dysregulation syndrome due to cytotoxic T-lymphocyte antigen 4 (CTLA-4) deficiency responsive to Abatacept therapy
Samuel Balbeur, Clinique Saint-Pierre Ottignies

PW 6

Recurrent tracheoesophageal fistula after repair of a congenital esophageal atresia. A challenging therapeutic and diagnostic journey: A case report
Sarah Eylenbosch, UZ Brussel

PW 7

Post-Infections bronchiolitis obliterans: 3 cases reports
Celine Kempeneers, CHU Liège

PW 8 

When the parasite travels with the man!
Sandy Finocchiaro, U Liège

PW 9 

Infectious Bronchiolitis, foreign body aspiration or both ? A case report
Johan Marchand, UZ Brussel

PW 10 

Wheezing episodes in children before and after the start of the COVID-19 pandemic in Brussels
Clémentine Delporte, ULB

PW 21

Clinical case of perinatal hydrometrocolpos: diagnosis and initial handling
Odile Hilgers, UCL

PW 41

Case report: Intracranial complications of acute sinusitis in children
Olil Van Reeth, U Liège

Thursday 16 March - Posterwalk 2 (PW 11 - PW 20)
13:00 - 13:30

PW 11

Asymmetric crying facies: writing on the wall?
Julie Messiaen, UZ Leuven

PW 12

Case report: Severe Neonatal Methylmalonic Acidemia associated with a heterozygous 5- Deoxyadenosylcobalamin A gene mutation
Veronica Carvalho, ULB

PW 13

Late metastatic relapse of an initially bifocal intracranial germ cell tumor in a 12-year-old child with modestly elevated tumor markers 
Emma Verdonck Beatove, U Liège

PW 14

A Rare Case of Congenital Sideroblastic Anemia in an Infant
Amelie Krug, ULB

PW 15

Granulocytic sarcoma of the pancreas: a very rare manifestation of acute myeloid leukemia in children 
Valérie Somerhausen, UCL

PW 16

A genetic syndrome unknown to practitioners
Noa Rager, HUDERF

PW 17

A case of LRBA deficiency with persistent immune dysregulation posttransplant 
Delfien Bogaert, UZ Gent

PW 18

A case of SETD2 mutation : a new clinically recognizable syndrome ?
Isabel Giménez Laso, UCL

PW 19

Growing-up with a complex congenital cardiac disease
Lorène Laurent, U Liège

PW 20

The efficacy of the use of atropine in children with pallid breath holding spells: can cardiac pacemaker implantation be avoided?
Marieke Donné, UZ Gent

Friday 17 March - Posterwalk 3 (PW 21 - P 30)
10:30 - 11:00

PW 22

Differential diagnosis of CNO/CRMO: a case report
Lieselot Peremans, U Gent

PW 23

A qualitative study on the knowledge and attitude of primary school students towards pediculosis capitis
Myrthe Daenen, UZ Leuven

PW 24

Robert Müler, CH Mouscron

PW 25

Clinical decision support through mobile applications: a systematic assessment of pediatric fever management apps.
Chloé Joosen, UZ Leuven

PW 26

Neonatal appendicitis : A diagnostic pitfall in a preterm neonate.
France Chalon, CHR Sambre et Meuse Namur

PW 27

Lize De Belder, UZ Brussel

PW 28

Exploring parental thoughts and clinical experiences on blended food in a pediatric population, a qualitative study
Rosalinde Verheije, UZ Leuven

PW 29 

Rehabilitation for pediatric patients with chronic functional complaints
An Schillemans, Zeepreventorium

PW 30

Diffuse large B-cell lymphoma as lead point for an ileocecal intussusception in a 4 year old boy: a case report and literature review.
Olivier Grognard, UZ Brussel

Friday 17 March - Posterwalk 4 (PW 31 - P 40) 
13:30 - 14:00

PW 31

An Update on Somatic Inpatient Treatment of Anorexia Nervosa: A Comparison of International Clinical Guidelines.
Martine Docx, Independant Researcher

PW 32

When hypercalcemia reveals an unusual diagnosis
Alexandra Losada-Espinedo, ULB

PW 33

Familial Renal Glucosuria Due to Mutations in the SLC5A2 Gene in a Male Adolescent.
Martine Docx, Independent Researcher

PW 34

An unusual severe acute kidney injury requiring prolonged dialysis in a 5 months old girl with a thrombotic thrombocytopenic purpura
Marie Longton, U Liège

PW 35

Congenital hyperinsulinism due to a new mutation in the gene ABCC8
Sophie Kaschten, U Liège

PW 36

The relationship between HbA1c and Time in Range during the preceding 2, 4 and 12 weeks in a paediatric population
Hanne Matheussen, KU Leuven

PW 37

A diabetes can hide another: always think about type 1 diabetes in children
Sylvie Tenoutasse, HUDERF

PW 38

Ectopic adrenocortical adenoma : a rare cause of hirsutism and hyperandrogenism
Lore Therssen, Jessa Ziekenhuis Hasselt

PW 39

Pendred syndrome: a rare cause of hypothyroidism with goiter and sensorineural hearing impairment
Gilles Tourlamain, UZ Gent

PW 40

Extreme short stature with microcephaly after intra-uterine growth retardation : a challenging diagnosis.
Marlon van Weelden, UZ Brussel