Juberg-Hayward syndrome

MeSH: C537690ORPHA: 2319

Contents

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

Overview

Juberg-Hayward syndrome is a polymalformative syndrome that associates multiple skeletal anomalies with microcephaly, facial dysmorphism, urogenital anomalies and intellectual deficit

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 Juberg-Hayward syndrome, sourced from HPO and Orphanet clinical annotations.

MicrocephalyWide noseIntrauterine growth retardationSevere short statureHypospadiasHorseshoe kidneyOrofacial cleftHypertelorismAbnormal eyebrow morphologyAbnormal rib morphologyAbnormal finger morphologyIntellectual disabilityHammertoeToe syndactylyHighly arched eyebrowScoliosisRadioulnar synostosisHypoplasia of the radiusAbnormality of the wristAbnormal vertebral morphologyAbnormal metacarpal morphologyShort thumbAbnormality of the elbowPtosisDandy-Walker malformationAnteriorly placed anus

Classification & Codes

MeSH Code

C537690

Orphanet Code

ORPHA:2319

Juberg-Hayward syndrome

MeSH	`C537690`
Orphanet	`ORPHA:2319`
Treatments	0 drug(s)
Symptoms on record	26 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO