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Feingold syndrome

MeSH: C537734ORPHA: 1305

Contents

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

Overview

autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation

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 Feingold syndrome, sourced from HPO and Orphanet clinical annotations.

Abnormal pinna morphologyMicrocephalyBrachydactylyClinodactyly of the 5th fingerDeviation of the 2nd fingerShort palpebral fissureMicrognathiaAnteverted naresIntellectual disabilityToe syndactylyHallux valgusShort statureDepressed nasal bridgeOrofacial cleftSensorineural hearing impairmentPatent ductus arteriosusAnnular pancreasAbnormality of the spleenEsophageal atresiaDuodenal atresiaAbnormal form of the vertebral bodies

Classification & Codes

MeSH Code

C537734

Orphanet Code

ORPHA:1305
Feingold syndrome
MeSHC537734
OrphanetORPHA:1305
Treatments0 drug(s)
Symptoms on record21 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO