Origenes embriológicos de los distintos tejidos.
神経クリストパチー：
3MC：3MC症候群、 アダルト: アダルト症候群、 紀元前：AEC症候群、 アラジール：アラジール症候群、 掲示板: バルデ・ビードル症候群 8、 BOR: 分枝耳腎症候群、 カダシル; CDHS: 頭蓋顔面難聴手症候群、 CED：頭蓋外胚葉異形成/ゼンセンブレンナー症候群、 EEC3：EEC3症候群、 EVC: エリス・ヴァン・クレヴェルド症候群、 FASD: 胎児性アルコールスペクトラム障害、 GDFD: 成長遅延、発達遅延、顔面異形症、 H.C.S.: ハイドゥ・チェイニー症候群、 H.E.D.: 発汗性低下性外胚葉異形成症、 HTX ヘテロタキシー、 KFS: クリッペル・ファイル症候群、 LMS: 四肢乳房症候群; MFDA: 脱毛症を伴う下顎顔面異形成症、 MPKU: 母体性 PKU 症候群、 MS。： 多発性硬化症、 NAD: ネイガー・アクロ顔面異骨症、 NS：ヌーナン症候群、 PA: ピーターズ・アノマリー、 フェーズ：PHACE症候群、 サムス：SAMS障害、 SHFM4: 分割手・分割足奇形タイプ 4、 SRTD: 短肋骨胸部異形成 10、 T.D.O.：毛根歯骨症候群。 プレビュー レビューに記載されている古典的な NCP の略語 (黒): 22q11：22q11.2欠失症候群。 AAA: アカラシア・アディソニア症・アラクリマ症候群、 ACS: 耳介顆症候群、 アルス: アクセンフェルト・リーガー症候群、 B.L.S.: バンフォース・ラザロ症候群、 BOFS: 分枝眼顔面症候群、 理学士: バインダー症候群; CCHS：先天性中枢性低換気症候群、 充電：CHARGE症候群、 CMT: シャルコー・マリー・トゥースおよび難聴症候群、 CS: 頭蓋骨癒合症、 D.B.A.：ダイアモンドブラックファン貧血、 F.D.：家族性自律神経失調症、 FMTC: 家族性甲状腺髄様癌、 GCMN：巨大な先天性メラノサイト母斑、 HH: 低性腺刺激性性腺機能低下症、 HPE: 全前脳症、 HSCR: ヒルシュスプルング病、 黒色腫; MBS：メビウス症候群、 MKS メッケル・グルーバー症候群、 MWS: モワット・ウィルソン症候群、 注：： 神経芽細胞腫、 NF1: 神経線維腫症 I, OAVS: 眼耳介脊椎症候群、 ガチョウ: 眼皮膚白皮症、 OFD: 口腔デジタル症候群、 PCC: 褐色細胞腫、 斑状禿げ症; ポッド: 軸後顔面骨形成不全症候群、 PRS: ピエール・ロバンのシーケンス、 SWS: スタージ・ウェーバー症候群、 タズ: ティーツ白皮症難聴症候群、 TCS: トリーチャー・コリンズ症候群、 VHL: フォン・ヒッペル・リンダウ症候群、 W.S.：ワールデンブルグ症候群。
19955111 {19955111:4L22XLA9} 1 バンクーバー 50 デフォルト 2754 https://neuropediatoolkit.org/wp-content/plugins/zotpress/
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1.
ベガロペスGA、セリスエラS、トリビュロC、アイバルMJ。神経堤病変：神経堤の発見から 150 年後の新たな洞察。発生生物学 [インターネット]。 2018年 [2018年11月12日引用];以下から入手可能: https://linkinghub.elsevier.com/retrieve/pii/S0012160617308382
神経クリスタパチーの放射線学。

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

rg.2019190086放電