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Related to Crouzon syndrome: Pfeiffer syndrome, Treacher Collins syndrome
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From the Same But Different project, left, Isabel Gardner, aged six, from Flint, has encephalitis, centre, Matthew Hogg, eight, from Mold, has Crouzon syndrome, and, right, Natalia Traista, 13, from Hope, has Patau syndrome
Among those being treated is two-year-old Coral who suffers from Crouzon syndrome, a rare genetic disorder that causes her brain to grow through her skull.
Any syndrome involving midface hypoplasia, such as Pierre-Robin sequence or Crouzon syndrome produces similar results and is at higher risk for developing SDB.
We took her to see many doctors and eventually she was diagnosed with Crouzon syndrome.
The PCR was performed by amplifying 50-100 ng of genomic DNA in a Human genes: FGFR2, fibroblast growth factor receptor 2 (bacteriaexpressed kinase, keratinocyte growth factor receptor, craniofacial dysostosis 1, Crouzon syndrome, Pfeiffer syndrome, Jackson-Weiss syndrome); FGFR3, fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism); TWISTI, twist homolog 1 (acrocephalosyndactyly 3; Saethre-Chotzen syndrome) (Drosophila); MSX2, rush homeobox 2; EFNBI, ephrin-B1; ALPL, alkaline phosphatase, liver/bone/kidney.
Twelve-year-old Ellie has Crouzon Syndrome, a rare and painful genetic condition that causes abnormal restraints on the growth of the skull, and undergoes life-saving surgery to relieve the pressure on her brain.
Abby was born with Crouzon Syndrome, which affects one in 60,000 babies born in the UK.
Recurrence of Bacterial Meningitis in a Patient With Crouzon Syndrome and Pseudomeningocele
Jonathan spent 15 minutes with threeyear-old Stanley Turner, born with Crouzon Syndrome, which causes the skull and facial bones to fuse together too early.