Patients Eligible
Thank you for your interest in being part of the FGFR Syndromes Research Registry- fgfr.iamrare.org
If you or your loved one has any of the following Syndromes you qualify to be part of the FGFR Syndromes Research Registry:
- Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
- Apert syndrome
- Beare-Stevenson cutis gyrata syndrome
- Bent bone dysplasia syndrome
- CATSHL syndrome (Camptodactyly, tall stature, and hearing loss syndrome)
- Crouzon syndrome
- Crouzon syndrome with acanthosis nigricans
- Hartsfield syndrome (holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate)
- Hypogonadotropic hypogonadism 2 with or without anosmia (Kallmann syndrome with anosmia)
- Jackson-Weiss syndrome
- LADD syndrome (Lacrimoauriculodentodigital syndrome)
- Muenke syndrome
- Osteoglophonic dysplasia
- Pfeiffer syndrome, type 1, 2 and 3
- Thanatophoric dysplasia, type I and 2

