You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 hub →Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 is a rare condition. Also known as Pascual-Castroviejo syndrome type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1394 · OMIM 213980, 616994 · ICD-10 Q87.5 · GARD 0001210
Start by learning the basics from an authoritative source, find a specialist or center that sees Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1, filtered to your area.
Tomeko shows live, recruiting studies for Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 from ClinicalTrials.gov on the hub.