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There is a page named "Craniofrontonasal syndrome" on Wikipedia
Craniofrontonasal dysplasia (craniofrontonasal syndrome, craniofrontonasal dysostosis, CFND) is a very rare X-linked malformation syndrome caused by mutations...20 KB (1,867 words) - 05:59, 14 July 2024
de Lange syndrome Craniofacial dysplasia-osteopenia syndrome Craniofrontonasal syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Crouzon...14 KB (1,403 words) - 01:56, 7 June 2024- Craniofaciocardioskeletal syndrome Craniofaciocervical osteoglyphic dysplasia Craniofrontonasal dysplasia Craniofrontonasal syndrome Teebi type Craniometaphyseal...40 KB (3,648 words) - 19:46, 6 May 2024
- CHARGE syndrome, familial dysautonomia, DiGeorge syndrome, Axenfeld-Rieger syndrome, Goldenhar syndrome (a.k.a. hemifacial microsomia), craniofrontonasal syndrome...6 KB (714 words) - 02:38, 19 March 2024
Mutations in this protein are responsible for most cases of craniofrontonasal syndrome. EFNB1 has been shown to interact with SDCBP. GRCh38: Ensembl...9 KB (1,097 words) - 20:34, 23 August 2023
junction communication at ectopic Eph/ephrin boundaries underlies craniofrontonasal syndrome". PLOS Biology. 4 (10): e315. doi:10.1371/journal.pbio.0040315...173 KB (17,264 words) - 08:00, 8 May 2024- of the STARD8 gene occurs in cases of craniofrontonasal syndrome where the EFNB1 gene (which causes the syndrome) is completely deleted. GRCh38: Ensembl...6 KB (816 words) - 12:32, 20 January 2024
Frontonasal dysplasia (redirect from Oculoauriculofrontonasal syndrome)inheritance pattern. The syndrome is often seen in siblings and, most of the time, parents are carriers. See Genetics. Craniofrontonasal dysplasia (CFND) is...27 KB (3,457 words) - 16:32, 5 January 2024
Loeys–Dietz syndrome. Hypertelorism can also be seen in Apert syndrome, Autism spectrum disorder, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis...10 KB (1,104 words) - 10:00, 2 June 2024- List of conditions with craniosynostosis (category Syndromes affecting head size)osteopenia syndrome (Concept Id: C1970027)". www.ncbi.nlm.nih.gov. Retrieved 2023-07-02. "Craniofrontonasal dysplasia-Poland anomaly syndrome (Concept Id:...52 KB (2,779 words) - 19:17, 14 October 2023
a set of characteristic physiological features which define whether a syndrome is a ciliopathy. Although ciliopathies are usually considered to involve...35 KB (2,499 words) - 18:40, 12 July 2024- morphogenesis and that defects in the human gene (EFNB1) lead to Craniofrontonasal Syndrome (CFNS). A different project has connected the cytoplasmic multi-PDZ...4 KB (531 words) - 03:11, 13 January 2024
- Cranioectodermal dysplasia; 218330; IFT122 Craniofacial-deafness-hand syndrome; 122880; PAX3 Craniofrontonasal dysplasia; 304110; EFNB1 Cranio-lenticulo-sutural dysplasia;...234 KB (18,877 words) - 15:43, 9 May 2024
- spectrum Frontofacionasal dysostosis - autosomal recessive inheritance Craniofrontonasal dysplasia Children's Craniofacial Association (CCA) Phone: (800) 535-3643