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Eng-Strom syndrome

ORPHA: 1937

Contents

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

Overview

Eng-Strom syndrome is characterised by intrauterine growth retardation and intermittent locking of the finger joints. It has been described in two individuals: a mother and her daughter. The mode of transmission is autosomal dominant.

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 Eng-Strom syndrome, sourced from HPO and Orphanet clinical annotations.

Pectus excavatumBrachydactylyArthritisIntrauterine growth retardationVentricular septal defectAbnormal cardiac septum morphologyScoliosisShort statureCamptodactyly of finger

Classification & Codes

Orphanet Code

ORPHA:1937
Eng-Strom syndrome
OrphanetORPHA:1937
Treatments0 drug(s)
Symptoms on record9 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO