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congenital absence of rib 相关文献:
Evaluation of congenital rib anomalies with multi-detector computed tomography in the Turkish population.
Oner Z, Oner S, Sahin NE, Cay M.
Folia Morphol (Warsz). 2024;83(1):182-191. doi: 10.5603/FM.a2023.0006. Epub 2023 Feb 16.
PMID:36794687
Reverse, innervated latissimus dorsi flap reconstruction of congenital diaphragmatic absence.
Wallace CA, Roden JS.
Plast Reconstr Surg. 1995 Sep;96(4):761-9. doi: 10.1097/00006534-199509001-00001.
PMID:7652049
Unilateral rib agenesis: antenatal three-dimensional ultrasonographic detection of the rare congenital anomaly of ribs.
Chauhan RS, Mane A, Kathrani N.
J Ultrasound. 2025 Mar;28(1):257-260. doi: 10.1007/s40477-024-00952-2. Epub 2024 Sep 20.
PMID:39302599
Reconstruction of Congenital Arhinia With Stereolithographic Modeling: Case Correlate and Literature Review.
Harrison LM, Anderson SR, Spiller KE, Pak KY, Schmidt SP, Mancho SN.
Cleft Palate Craniofac J. 2022 Apr;59(4):530-537. doi: 10.1177/10556656211012859. Epub 2021 Jul 22.
PMID:34291675
ABSENCE OF A RIB IN DOWN'S SYNDROME.
BEBER BA.
Lancet. 1965 Aug 7;2(7406):289. doi: 10.1016/s0140-6736(65)92413-x.
PMID:14332711
Osseous Thoracic Foraminal Stenosis with Unilateral Congenital Absence of T1 Rib A Case Report.
Wang C, Vira S, Stieber J.
Bull Hosp Jt Dis (2013). 2021;79(3):197-199.
PMID:34605758
Consideration of the thoracic phenotype of cerebro-costo-mandibular syndrome.
Keeling H, Williams EJ, Itasaki N.
Clin Anat. 2024 Apr;37(3):254-269. doi: 10.1002/ca.24054. Epub 2023 Jun 2.
PMID:37265362
Radiological and histopathological features of short rib-polydactyly syndrome type III and identification of two novel DYNC2H1 variants.
Xia CL, Xiao SQ, Yang X, Liu CX, Qiu H, Jiang HK, Li-Ling J, Lyu Y.
Mol Med Rep. 2021 Jun;23(6):426. doi: 10.3892/mmr.2021.12065. Epub 2021 Apr 13.
PMID:33846808
An Unusual Delayed Complication of Rib Graft Microtia Reconstruction After Two Decades: A Case Report.
Tuang GJ, Mansor M, Abdullah A.
Indian J Otolaryngol Head Neck Surg. 2022 Dec;74(Suppl 3):3671-3674. doi: 10.1007/s12070-020-02316-8. Epub 2021 Jan 25.
PMID:36742599
A novel NEK1 variant disturbs the interaction between the C-terminal fragment of NEK1 and the VDAC1 channel, causing lethal short-rib polydactyly syndrome.
Gruca-Stryjak K, Maciak K, Winiewska-Szajewska M, Jurkiewicz A, Gora M, Kacprzak MM, Drgas O, Bialek-Proscinska A, Sobczynska-Tomaszewska A, Pluta KD, Jamsheer A, Markwitz W, Poznanski J, Burzynska B.
Bone. 2025 Jun;195:117471. doi: 10.1016/j.bone.2025.117471. Epub 2025 Mar 25.
PMID:40147672
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