OrphanDrug
OrphanDrug
Pharma Knowledge Base

Pierre Robin syndrome

ICD-10: Q87.0MeSH: D010855ORPHA: 2432

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

a congenital condition with micrognathia and glossoptosis

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with Pierre Robin syndrome, sourced from HPO and Orphanet clinical annotations.

Abnormal cranial suture/fontanelle morphologyBroad foreheadMicrocorneaMicrophthalmiaLarge for gestational ageRecurrent respiratory infectionsHepatomegalyRespiratory insufficiencyAbnormal calvaria morphologyCorneal opacityMedian cleft palatePtosisCraniosynostosisHypotelorismGlossoptosis

Classification & Codes

ICD-10 Code

Q87.0

MeSH Code

D010855

Orphanet Code

ORPHA:2432
Pierre Robin syndrome
ICD-10Q87.0
MeSHD010855
OrphanetORPHA:2432
Treatments0 drug(s)
Symptoms on record15 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO