Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Search help
122 results
  1. Birth Defects 
    https://medlineplus.gov/birthdefects.html
    A birth defect is a problem that happens while a baby is developing in the mother's body. Learn about the different types of birth defects, their treatments, ...
  2. Brain Malformations 
    https://medlineplus.gov/brainmalformations.html
    Brain malformations is damage or abnormal development of the brain and nervous system. Starts long before a baby is born. Learn types and treatments. ... Most ...
  3. Esophageal atresia/tracheoesophageal fistula 
    https://medlineplus.gov/...phageal-atresia-tracheoesophageal-fistula
    ... Atresia / Tracheoesophageal Fistula Overview - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 2009 Mar 12 [updated 2018 Sep 20]. ...
  4. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... topic><topic ><url >https://medlineplus.gov/genetics/condition/trisomy-13</url><title >Trisomy 13</title><other_names ><other_name >Bartholin-Patau syndrome</ ...
  5. Prenatal Cell-Free DNA Screening: MedlinePlus Medical Test 
    https://medlineplus.gov/lab-tests/prenatal-cell-free-dna-screening
    ... extra copy of chromosome 18, and Patau syndrome (trisomy 13) , where there is an extra copy of chromosome ... Down syndrome. Most babies with trisomy 18 or trisomy 13 die within the first year of life. There ...
  6. Holoprosencephaly Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1530
    ... severe clinical course in most. Numeric chromosome abnormalities. Trisomy 13, the most common cause of HPE, is observed ... HPE caused by chromosome abnormalities. Birth prevalence of trisomy 13 is 1:5000. Arrhinencephaly is seen in about ...
  7. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... Rubinstein-Taybi Syndrome C10.597.606.360.835 Trisomy 13 Syndrome C10.597.606.360.969 WAGR Syndrome ... 960 Trilogy of Fallot C14.240.400.970 Trisomy 13 Syndrome C14.240.400.975 Trisomy 18 Syndrome ...
  8. Primary Congenital Glaucoma - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1135
    ... may not be compatible with life (e.g., trisomy 13, trisomy 18, Walker-Warburg syndrome, and Zellweger Syndrome ); others ... posted live 3 June 2004 (bab) Original submission References Literature Cited Abu-Amero KK, Morales J, Aljasim ...
  9. Wilms Tumor Predisposition - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1294
    ... Syndromes That May Be Associated with Wilms Tumor Trisomy 13 and trisomy 18 (both characterized by multiple congenital ... posted live 14 July 2003 (jsd) Original submission References Literature Cited Beckwith JB. Children at increased risk ...
  10. Smith-Lemli-Opitz Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1143
    ... following (shared clinical findings are indicated in parentheses): Trisomy 13 syndrome (holoprosencephaly, cleft lip and cleft palate, cardiac ... by TL Kurtzman, BA and C Cunniff, MD References Literature Cited Abuelo DN, Tint GS, Kelley R, ...
first · previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next · last