Yunis-Varon syndrome
MeSH: C536719ORPHA: 3472
Overview
Human disease
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 Yunis-Varon syndrome, sourced from HPO and Orphanet clinical annotations.
Aplasia of distal finger phalanxAplasia of the distal phalanx of the halluxShort proximal phalanx of halluxHypospadiasMicropenisShort upper lipBroad secondary alveolar ridgeThin vermilion borderDolichocephalyHypertelorismShort philtrumShort chinMicrognathiaHigh foreheadLow-set earsAbnormal pinna morphologyAnteverted naresCataractProptosisUpslanted palpebral fissureSclerocorneaSparse eyelashesSingle transverse palmar creaseSyndactylyAbnormal finger morphologyTapered fingerGlobal developmental delayAgenesis of corpus callosumPachygyriaSevere failure to thriveVentricular septal defectCardiomyopathyCardiomegalyShort toeRocker bottom footMetatarsus adductusPulmonary arterial hypertensionArrhinencephalySparse scalp hairNeuronal loss in central nervous systemAbnormal parietal bone morphologyHigh, narrow palateShort statureDecreased skull ossificationShortening of all distal phalanges of the toesShort middle phalanx of fingerRedundant neck skinPremature loss of primary teethAbsent sternal ossificationAplasia/Hypoplasia of the nipplesAplasia/Hypoplasia of the claviclesHypoplasia of the frontal lobesBilateral microphthalmosAplasia/Hypoplasia of the nailsPostnatal growth retardationGeneralized neonatal hypotoniaShort fingerAbsent thumbAplasia of the 1st metacarpalAplasia/hypoplasia of the 1st metatarsalWide cranial suturesAbnormality of dental structurePrimary microcephalyAbnormal occipital bone morphologyAbnormal pelvis bone morphologySparse eyebrowCryptorchidismHypoplastic labia majoraGlossoptosisHydrocephalusHearing impairmentMicrophthalmiaShort ribsHypertensionCerebellar hypoplasiaPolyhydramniosAtrial septal defectHydrops fetalisRenal artery stenosisPyloric stenosisHip dislocationFlared metaphysisSlender long bones with narrow diaphysesAplasia/Hypoplasia of the scapulaeClitoral hypertrophyIncreased nuchal translucencyNarrow nasal baseGingival recessionRenovascular hypertensionTetralogy of Fallot
Classification & Codes
MeSH Code
C536719Orphanet Code
ORPHA:3472Yunis-Varon syndrome
| MeSH | C536719 |
| Orphanet | ORPHA:3472 |
| Treatments | 0 drug(s) |
| Symptoms on record | 90 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO