Origenes embriológicos de los distintos tejidos.
Neurocristopatías:
3MC: 3MC Syndrome, ADULT: ADULT syndrome, AEC: AEC Syndrome, Alagille: Alagille Syndrome, BBS: Bardet-Biedl Syndrome 8, BOR: Branchio-Oto-Renal Syndrome, CADASIL; CDHS: Craniofacial-Deafness-Hand Syndrome, CED: Cranioectodermal dysplasia/Sensenbrenner syndrome, EEC3: EEC3 syndrome, EVC: Ellis-van Creveld syndrome, FASD: Fetal Alcohol Spectrum Disorder, GDFD: Growth Retardation, Developmental Delay, and Facial Dysmorphism, HCS: Hajdu-Cheney Syndrome, HED: Hypohidrotic Ectodermal Dysplasia, HTX Heterotaxy, KFS: Klippel-Feil Syndrome, LMS: Limb-Mammary Syndrome; MFDA: Mandibulofacial Dysostosis with Alopecia, MPKU: Maternal PKU syndrome, MS: Multiple sclerosis, NAD: Nager Acrofacial Dysostosis, NS: Noonan syndrome, PA: Peters Anomaly, PHACE: PHACE Syndrome, SAMS: SAMS disorder, SHFM4: Split-hand/split-foot malformation type 4, SRTD: Short-Rib Thoracic Dysplasia 10, TDO: Tricho-dento-osseous syndrome. Abbreviations of classical NCP described in previews reviews (black): 22q11: 22q11.2 Deletion Syndrome; AAA: Achalasia-Addisonianism-Alacrima Syndrome, ACS: Auriculo Condylar Syndrome, ARS: Axenfeld-Rieger Syndrome, BLS: Bamforth-Lazarus syndrome, BOFS: Branchio-Oculo-Facial Syndrome, BS: Binder Syndrome; CCHS: Congenital Central Hypoventilation Syndrome, CHARGE: CHARGE syndrome, CMT: Charcot-Marie-Tooth and Deafness Syndrome, CS: Craniosynostosis, DBA: Diamond Blackfan Anemia, FD: Familial dysautonomia, FMTC: Familial Medullary thyroid carcinomas, GCMN: Giant congenital melanocytic nevi, HH: Hypogonadotropic Hypogonadism, HPE: Holoprosencephaly, HSCR: Hirschsprung Disease, Melanoma; MBS: Moebius Syndrome, MKS Meckel-Gruber syndrome, MWS: Mowat Wilson Syndrome, NB: Neuroblastoma, NF1: Neurofibromatosis I, OAVS: Oculo-Auriculo-Vertebral Syndrome, OCA: Oculocutaneous Albinism, OFD: Orofaciodigital Syndrome, PCC: Pheochromocytomas, Piebaldism; POADS: Postaxial Acrofacial Dysostosis Syndrome, PRS: Pierre Robin sequence, SWS: Sturge-Weber syndrome, TADS: Tietz Albinism-Deafness Syndrome, TCS: Treacher Collins Syndrome, VHL: von Hippel-Lindau Syndrome, WS: Waardenburg Syndrome.
1.
Vega-Lopez GA, Cerrizuela S, Tribulo C, Aybar MJ. Neurocristopathies: New insights 150 years after the neural crest discovery. Developmental Biology [Internet]. 2018 [cited 2018 Nov 12]; Available from: https://linkinghub.elsevier.com/retrieve/pii/S0012160617308382
Radiología de las neurocristopatías.

https://pubs.rsna.org/doi/full/10.1148/rg.2019190086

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