POSTERWALK SESSIONS

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

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

COMPLICATION OF CHICKENPOX: OSTEITIS AND VENOUS THROMBOSIS IN IMMUNOCOMPETENT CHILDREN
Ivana Lion, U Liège

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

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

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

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

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

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

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

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

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

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

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

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

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

A genetic syndrome unknown to practitioners
Noa Rager, HUDERF

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

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

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

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

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

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

BILATERAL PULMONARY EMBOLISM IN A TEENAGE GIRL
Robert Müler, CH Mouscron

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

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

BLENDERIZED TUBE FEEDING FOR CHILDREN: A SYSTEMATIC REVIEW OF THE IMPACT ON UPPER GASTRO-INTESTINAL SYMPTOMS
Lize De Belder, UZ Brussel

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

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

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

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

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

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

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

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

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

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

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

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

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