Camptodactyly syndrome, Guadalajara type 2

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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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024

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Camptodactyly syndrome, Guadalajara type 2?

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