POSTERWALK SESSIONS

                                                                                                                                                                       
Back to program Thursday Back to program Friday

Thursday 17 March - Posterwalk 1 (PW 1 - PW 10)
10:30 - 11:00 
  
PW 1

Group A Streptococcus meningitis: report of a case

PW 2

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

PW 3

COMPLICATION OF CHICKENPOX: OSTEITIS AND VENOUS THROMBOSIS IN IMMUNOCOMPETENT CHILDREN

PW 4

Acute dyspnea in a 7-year-old girl: From pearl to plague

PW 5

Immune dysregulation syndrome due to cytotoxic T-lymphocyte antigen 4 (CTLA-4) deficiency responsive to Abatacept therapy

PW 6

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

PW 7

Post-Infections bronchiolitis obliterans: 3 cases reports

PW 8 

When the parasite travels with the man!

PW 9 

Infectious Bronchiolitis, foreign body aspiration or both ? A case report

PW 10 

Wheezing episodes in children before and after the start of the COVID-19 pandemic in Brussels



Thursday 17 March - Posterwalk 2 (PW 11 - PW 20)
13:00 - 13:30

PW 11

Asymmetric crying facies: writing on the wall?

PW 12

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

PW 13

Late metastatic relapse of an initially bifocal intracranial germ cell tumor in a 12-year-old child with modestly elevated tumor markers 

PW 14

A Rare Case of Congenital Sideroblastic Anemia in an Infant

PW 15

Granulocytic sarcoma of the pancreas: a very rare manifestation of acute myeloid leukemia in children 

PW 16

A genetic syndrome unknown to practitioners

PW 17

A case of LRBA deficiency with persistent immune dysregulation posttransplant 

PW 18

A case of SETD2 mutation : a new clinically recognizable syndrome ?

PW 19

Growing-up with a complex congenital cardiac disease

PW 20

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


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

PW 21

Clinical case of perinatal hydrometrocolpos: diagnosis and initial handling

PW 22

Differential diagnosis of CNO/CRMO: a case report

PW 23

A qualitative study on the knowledge and attitude of primary school students towards pediculosis capitis

PW 24

BILATERAL PULMONARY EMBOLISM IN A TEENAGE GIRL

PW 25

Clinical decision support through mobile applications: a systematic assessment of pediatric fever management apps.

PW 26

Neonatal appendicitis : A diagnostic pitfall in a preterm neonate.

PW 27

BLENDERIZED TUBE FEEDING FOR CHILDREN: A SYSTEMATIC REVIEW OF THE IMPACT ON UPPER GASTRO-INTESTINAL SYMPTOMS

PW 28

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

PW 29 

Rehabilitation for pediatric patients with chronic functional complaints

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.



Friday 18 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.

PW 32

When hypercalcemia reveals an unusual diagnosis

PW 33

Familial Renal Glucosuria Due to Mutations in the SLC5A2 Gene in a Male Adolescent.

PW 34

An unusual severe acute kidney injury requiring prolonged dialysis in a 5 months old girl with a thrombotic thrombocytopenic purpura

PW 35

Congenital hyperinsulinism due to a new mutation in the gene ABCC8

PW 36

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

PW 37

A diabetes can hide another: always think about type 1 diabetes in children

PW 38

Ectopic adrenocortical adenoma : a rare cause of hirsutism and hyperandrogenism

PW 39

Pendred syndrome: a rare cause of hypothyroidism with goiter and sensorineural hearing impairment

PW 40

Extreme short stature with microcephaly after intra-uterine growth retardation : a challenging diagnosis.