chromosome 15q24 deletion syndrome
MeSH: C579849ORPHA: 94065
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 chromosome 15q24 deletion syndrome, sourced from HPO and Orphanet clinical annotations.
Joint hypermobilityScoliosisKyphosisDepressed nasal bridgeProximal placement of thumbIntestinal atresiaFeeding difficultiesWide nasal baseClinodactylyMicrophallusHerniaSmall handMyelomeningoceleGlobal developmental delayEpicanthusSmooth philtrumLong philtrumAbnormality of the outer earDownslanted palpebral fissuresAtypical behaviorBrachydactylyIntellectual disabilityHypotoniaSmall for gestational ageRecurrent infectionsShort staturePostnatal growth retardationHigh anterior hairlineBroad eyebrowCryptorchidismHypospadiasNarrow mouthAbnormality of the dentitionAbnormal palate morphologyThick lower lip vermilionMicrocephalyLong faceHypertelorismFacial asymmetryHearing impairmentProminent nasal bridgeStrabismusColobomaNystagmusCongenital diaphragmatic herniaDecreased response to growth hormone stimulation testAbnormal thumb morphologyFailure to thriveObesityAbnormal heart morphologyAbnormal toe morphologyAnal atresia
Classification & Codes
MeSH Code
C579849Orphanet Code
ORPHA:94065chromosome 15q24 deletion syndrome
| MeSH | C579849 |
| Orphanet | ORPHA:94065 |
| Treatments | 0 drug(s) |
| Symptoms on record | 52 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO