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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Pfeiffer Tietze Welte syndrome


Other Names for this Disease
  • Sagittal craniostenosis, bilateral coloboma of the iris, craniofacial dysmorphy, asymmetrical split hand malformation, bilateral syndactyly of 2nd-4th
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Overview


These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.

Your Questions Answered
by the Genetic and Rare Diseases Information Center

Please contact us with your questions about Pfeiffer Tietze Welte syndrome. We will answer your question and update these pages with new resources and information.

Basic Information

  • The Children’s Hospital Boston has a information page on congenital limb defects. Click on the link above to view this information page.
  • More information on limb abnormalities can be found at the following link from MEDLINEplus, the National Library of Medicine Web site designed to help you research your health questions.

In Depth Information

  • PubMed is a searchable database of medical literature and lists journal articles that discuss Pfeiffer Tietze Welte syndrome. Click on the link to view a sample search on this topic.