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