Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2015 1
2017 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

3 results

Results by year

Filters applied: . Clear all
Page 1
Congenital lesions of epithelial origin.
Hills SE, Maddalozzo J. Hills SE, et al. Otolaryngol Clin North Am. 2015 Feb;48(1):209-23. doi: 10.1016/j.otc.2014.09.014. Otolaryngol Clin North Am. 2015. PMID: 25439555 Review.
Association of Recurrence of Infected Congenital Preauricular Cysts Following Incision and Drainage vs Fine-Needle Aspiration or Antibiotic Treatment: A Retrospective Review of Treatment Options.
Rataiczak H, Lavin J, Levy M, Bedwell J, Preciado D, Reilly BK. Rataiczak H, et al. JAMA Otolaryngol Head Neck Surg. 2017 Feb 1;143(2):131-134. doi: 10.1001/jamaoto.2016.2988. JAMA Otolaryngol Head Neck Surg. 2017. PMID: 27787535
Children treated for preauricular sinus tract infections were identified using the procedure code for excision of preauricular pit, cyst, or sinus tract. MAIN OUTCOMES AND MEASURES: Postexcision recurrence. ...Our results suggest a more conservative treatment of inf …
Children treated for preauricular sinus tract infections were identified using the procedure code for excision of preauricular pit
Apparent cyclophosphamide (cytoxan) embryopathy: a distinct phenotype?
Enns GM, Roeder E, Chan RT, Ali-Khan Catts Z, Cox VA, Golabi M. Enns GM, et al. Am J Med Genet. 1999 Sep 17;86(3):237-41. Am J Med Genet. 1999. PMID: 10482872 Review.
The infant had growth retardation and multiple anomalies including microbrachycephaly, coronal craniosynostosis, hypotelorism, shallow orbits, proptosis, blepharophimosis, small, abnormal ears, unilateral preauricular pit, broad, flat nasal bridge, microstomia, high …
The infant had growth retardation and multiple anomalies including microbrachycephaly, coronal craniosynostosis, hypotelorism, shallow orbit …