Failure to Thrive: An Expanded Differential Diagnosis.

Wolman's disease failure to thrive

Journal

Journal of pediatric genetics
ISSN: 2146-4596
Titre abrégé: J Pediatr Genet
Pays: Germany
ID NLM: 101589859

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 09 06 2018
accepted: 23 07 2018
entrez: 19 2 2019
pubmed: 19 2 2019
medline: 19 2 2019
Statut: ppublish

Résumé

The patient is a term 6-month-old male, who presented with failure to thrive since birth. History was remarkable for suspected milk and soy protein allergy, gastroesophageal reflux, constipation, and abdominal distension that was present since birth. He was losing weight despite oral intake of over 100 kcal/kg per day. Prior workup including laboratory studies, abdominal X-ray, upper gastrointestinal series with fluoroscopy, barium enema, and abdominal ultrasound were all within normal limits. The patient's history, diagnostic evaluation, and final diagnosis are revealed. This case highlights a rare condition presenting as failure to thrive, a common problem with a wide differential diagnosis.

Identifiants

pubmed: 30775051
doi: 10.1055/s-0038-1669445
pii: 1800029
pmc: PMC6375721
doi:

Types de publication

Case Reports

Langues

eng

Pagination

27-32

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Auteurs

Alexandra Lazzara (A)

Department of Pediatrics, Penn State Health Children's Hospital, Hershey, Pennsylvania, United States.
Department of Pediatrics, Johns Hopkins Children's Center, Baltimore, Maryland, United States.

Carrie Daymont (C)

Department of Pediatrics, Penn State Health Children's Hospital, Hershey, Pennsylvania, United States.

Roger Ladda (R)

Department of Pediatrics, Penn State Health Children's Hospital, Hershey, Pennsylvania, United States.

Jordan Lull (J)

Department of Pediatrics, Penn State Health Children's Hospital, Hershey, Pennsylvania, United States.

Can Ficicioglu (C)

Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States.

Jennifer L Cohen (JL)

Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States.

Justen Aprile (J)

Department of Pediatrics, Penn State Health Children's Hospital, Hershey, Pennsylvania, United States.

Classifications MeSH