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Items: 1 to 20 of 22

1.
Sacral Dimple, Conjunctiva, and Nipple as Less Obvious Pemphigus Vulgaris Locations around Natural Body Orifices: A Report of Three Cases
Magdalena Jałowska, Justyna Gornowicz-Porowska, Monika Bowszyc-Dmochowska, Marian Dmochowski
J Clin Med. 2022 May; 11(10): 2855. Published online 2022 May 18. doi: 10.3390/jcm11102855
PMCID:
PMC9146475
ArticlePDF–1.4M
2.
Outcome of ultrasonographic imaging in infants with sacral dimple
Jin Hyuk Choi, Taekwan Lee, Hyeok Hee Kwon, Sun Kyoung You, Joon Won Kang
Korean J Pediatr. 2018 Jun; 61(6): 194–199. Published online 2018 Jun 25. doi: 10.3345/kjp.2018.61.6.194
PMCID:
PMC6021363
ArticlePDF–1.0M
3.
Acute flaccid paralysis in a patient with sacral dimple
Mohammed Mostafa, Nehad Nasef, Tarik Barakat, Amany K El-Hawary, Hesham Abdel-Hady
World J Clin Pediatr. 2013 Aug 8; 2(3): 26–30. Published online 2013 Aug 8. doi: 10.5409/wjcp.v2.i3.26
PMCID:
PMC4145641
ArticlePDF–841K
4.
New report of two patients with mosaic trisomy 9 presenting unusual features and longer survival
Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa, Rosana Cardoso Manique Rosa, Carla Graziadio, Giorgio Adriano Paskulin
Sao Paulo Med J. 2011; 129(6): 428–432. Published online 2011 Dec 1. doi: 10.1590/S1516-31802011000600010
PMCID:
PMC10868921
ArticlePDF–507K
5.
Tethered Cord Syndrome: Role of Imaging Findings in Surgical Decision-Making
Nolan Otto, Jennifer Kucera, Laura L Hayes, Tushar Chandra
Cureus. 2023 Sep; 15(9): e44854. Published online 2023 Sep 7. doi: 10.7759/cureus.44854
PMCID:
PMC10560071
ArticlePDF–641K
6.
Co-occurrence of subcutaneous myxopapillary ependymoma, dermal sinus tract, and filum terminale lipoma: a review of the pathobiology of caudal spinal cord development and spinal cord tethering. Illustrative case
Gabrielle W. Johnson, Yuxiao Xu, Ali Y. Mian, David D. Limbrick, Jr
J Neurosurg Case Lessons. 2023 Jan 23; 5(4): CASE22451. Published online 2023 Jan 23. doi: 10.3171/CASE22451
PMCID:
PMC10550699
ArticlePDF–757K
7.
Reliability of Fossae Lumbales Laterales and Pelvic Incidence for Estimating Transsacral Corridors Assessed Using Reconstruction Computed Tomography
Orhan Balta, Mehmet Akif Yılmaz, Kürşad Aytekin, Recep Kurnaz, Harun Altinayak, Mehmet Burtaç Eren, Eyüp Çağatay Zengin
Clin Orthop Surg. 2022 Sep; 14(3): 417–425. Published online 2022 Jul 21. doi: 10.4055/cios22090
PMCID:
PMC9393270
ArticlePDF–1.7M
8.
A Case of Smith-Lemli-Opitz Syndrome Diagnosed with Hypertrophic Pyloric Stenosis
Elif Ece Eren, Nurbanu Bilgin, Nafiye Urganci, Gulsen Kose
Sisli Etfal Hastan Tip Bul. 2021; 55(2): 268–271. Published online 2021 Jul 2. doi: 10.14744/SEMB.2020.34651
PMCID:
PMC8298070
ArticlePDF–654K
9.
Split Cord Malformation Type 2 with Double Dorsal Lipoma: A Sequela or a Chance
Mohamed A Jamaluddin, Prakash Nair, Ganesh Divakar, Jaypalsinh A Gohil, Mathew Abraham
J Pediatr Neurosci. 2020 Apr-Jun; 15(2): 135–139. Published online 2020 Jun 27. doi: 10.4103/jpn.JPN_131_19
PMCID:
PMC7519753
Article
10.
Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion
Anudeep Yekula, Connor Grant, Mihir Gupta, David R. Santiago-Dieppa, Pate J. Duddleston, David Gonda, Michael Levy
Childs Nerv Syst. 2020; 36(7): 1367–1377. Published online 2020 May 12. doi: 10.1007/s00381-020-04642-2
PMCID:
PMC7300078
ArticlePDF–523K
11.
A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review
Bader Almuzzaini, Nasser S. Alatwi, Saif Alsaif, Mohammed A. Al Balwi
Mol Genet Genomic Med. 2020 Apr; 8(4): e1135. Published online 2020 Jan 28. doi: 10.1002/mgg3.1135
PMCID:
PMC7196451
ArticlePDF–501K
12.
Dermal Sinus Tract of Lumbosacral Spine in Children: Patterns on Magnetic Resonance Imaging and Scoring System
Jessica Lane, Mark Dias, Mark Iantosca, Thomas Zacharia, R. Shane Tubbs, Elias Rizk
Cureus. 2017 Dec; 9(12): e1906. Published online 2017 Dec 4. doi: 10.7759/cureus.1906
PMCID:
PMC6438690
ArticlePDF–108K
13.
Dorsal midline cutaneous stigmata associated with occult spinal dysraphism in pediatric patients
Hyun Jung Sung, Hyun-Seung Lee
Korean J Pediatr. 2019 Feb; 62(2): 68–74. Published online 2018 Oct 1. doi: 10.3345/kjp.2018.06744
PMCID:
PMC6382965
ArticlePDF–877K
14.
De novo interstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case
Ha-Su Kim, Jin-Yeong Han, Myo-Jing Kim
Korean J Pediatr. 2015 Aug; 58(8): 313–316. Published online 2015 Aug 21. doi: 10.3345/kjp.2015.58.8.313
PMCID:
PMC4573446
ArticlePDF–459K
15.
Cat eye syndrome
Deepak Sharma, Srinivas Murki, Tejo Pratap, Madhavi Vasikarla
BMJ Case Rep. 2014; 2014: bcr2014203923. Published online 2014 May 19. doi: 10.1136/bcr-2014-203923
PMCID:
PMC4039909
ArticlePDF–346K
16.
Congenital Uterovaginal Prolapse Present at Birth
Ekwunife Okechukwu Hyginus, Chukwuka Onuora John
J Surg Tech Case Rep. 2013 Jul-Dec; 5(2): 89–91. doi: 10.4103/2006-8808.128741
PMCID:
PMC3977332
ArticlePDF–501K
17.
A Cross-Sectional Prospective Study of Cutaneous Lesions in Newborn
Farhana Tahseen Taj Sameer Haveri, Arun C. Inamadar
ISRN Dermatol. 2014; 2014: 360590. Published online 2014 Jan 20. doi: 10.1155/2014/360590
PMCID:
PMC3918370
ArticlePDF–1.1M
18.
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions
Minire Hasi, Bridgette Soileau, Courtney Sebold, Annice Hill, Daniel E. Hale, Louise O’Donnell, Jannine D. Cody
Hum Genet. Author manuscript; available in PMC 2012 Dec 1.
Published in final edited form as: Hum Genet. 2011 Dec; 130(6): 777–787. Published online 2011 Jun 14. doi: 10.1007/s00439-011-1020-y
PMCID:
PMC3215814
ArticlePDF–1.7M
19.
Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1)
A. Utkus, I. Sorokina, V. Kucinskas, B. Rothlisberger, D. Balmer, L. Brecevic, A. Schinzel
J Med Genet. 1999 Jan; 36(1): 73–76.
PMCID:
PMC1762944
SummaryPDF–104K
20.
Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
S Ohdo, H Madokoro, T Sonoda, M Takei, H Yasuda, N Mori
J Med Genet. 1987 Oct; 24(10): 609–612. doi: 10.1136/jmg.24.10.609
PMCID:
PMC1050288
SummaryPage BrowsePDF–813K

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