Ramos-Arroyo syndrome
MeSH: C535286ORPHA: 1051
Overview
medical condition
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 Ramos-Arroyo syndrome, sourced from HPO and Orphanet clinical annotations.
Abnormal midface morphologyDecreased corneal sensationBroad faceHypertelorismKeratitisNasolacrimal duct obstructionUpslanted palpebral fissureIntellectual disabilitySevere failure to thrivePatent ductus arteriosusFrontal bossingDelayed gross motor developmentAganglionic megacolonSevere short statureDecreased body weightDepressed nasal bridgeReduced visual acuityAbsent retinal pigment epitheliumBilateral sensorineural hearing impairmentConcave nasal ridgeProminent foreheadAbnormal autonomic nervous system physiologyChoriocapillaris atrophyNarrow mouthXerostomiaLong philtrumChoanal stenosisAnteverted naresChorioretinal atrophyDacryocystitisCarious teethSelf-mutilationAtrial septal defectRespiratory distressSparse scalp hairDeviated nasal septumSleep-wake cycle disturbanceFeeding difficulties in infancyHigh anterior hairlineSmooth tongueShoulder dimplePrimary microcephalyChronic constipationFood intoleranceCorneal ulcerationNarrow palpebral fissure
Classification & Codes
MeSH Code
C535286Orphanet Code
ORPHA:1051Ramos-Arroyo syndrome
| MeSH | C535286 |
| Orphanet | ORPHA:1051 |
| Treatments | 0 drug(s) |
| Symptoms on record | 46 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO