camptodactyly syndrome, Guadalajara camptodactyly syndrome, Guadalajara type 2 https://rarediseases.info.nih.gov/diseases/1068/camptodactyly-syndrome-guadalajara-type-2 https://www.malacards.org/card/camptodactyly_syndrome_guadalajara_type_ii MONDO:0008899 GARD:0001068 Camptodactyly syndrome, Guadalajara type 2 is an extremely rare multiple congenital anomaly syndrome characterized by distinctive intrauterine growth retardation, skeletal dysplasia with multiple malformations including camptodactyly of all fingers, bilateral hallux valgus, short second, fourth and fifth toes, hypoplastic patella, microcephaly, low-set ears, short neck, cuboid-shaped vertebral bodies, pectus excavatum, hip dislocation, and hypoplastic pubic region and genitalia. Camptodactyly syndrome, Guadalajara type 2 has been described in two sisters and is most likely transmitted in an autosomal recessive manner. There have been no further descriptions in the literature since 1985. camptodactyly syndrome Guadalajara type 2 Guadalajara camptodactyly syndrome type II OMIM:211920 MESH:C567138 SCTID:720603002 Orphanet:1326 MEDGEN:419870 UMLS:C2931680 multiple congenital anomalies/dysmorphic syndrome without intellectual disability dysostosis congenital limb malformation