Guide to Jewish Living : Reproductive Genetics Innovations 2026

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  1. Click ‘Get Form’ to open it in the editor.
  2. Begin by filling out the Patient Information section. Enter the last and first names of both the patient and partner, along with their addresses, phone numbers, dates of birth, and last four digits of their Social Security Numbers.
  3. In the Biopsy/Transfer/Batching Details section, specify whether a biopsy is needed and select options for transfer and batching as applicable.
  4. For Setup/Test Request(s), check all relevant tests such as Aneuploidy (PGT-A) or Single gene disorder (PGT-M) and provide any additional details regarding your testing strategy.
  5. Complete the Cycle Information section by confirming tentative and confirmed dates related to hCG.
  6. Fill in the ICD-10 Format with diagnosis/symptoms and relevant dates for stimulation start, retrieval, biopsy, and transfer/freeze.
  7. Provide IVF Center Information including name, address, referring physician details, and contact information.
  8. Lastly, indicate Billing Preferences and Reporting Preferences before submitting your form via email or fax as instructed.

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Screening is recommended for people who have at least one Jewish grandparent. This includes Sephardic and Mizrahi backgrounds as well as Ashkenazi Jews. There are genetic diseases that are more common in among Sephardim and Mizrahim. Its also recommended even if your partner is not Jewish.
The Ashkenazi Jewish screening panel currently consists of testing for seven diseases common in the Ashkenazi Jewish population: Bloom syndrome (BLM), Canavan disease (CVN), Familial dysautonomia (FD), Fanconi anemia group C (FA-C), Mucolipidosis type IV (MLP4), Niemann-Pick disease type A B (NP) and Tay-Sachs
The authors found that the closest genetic neighbors to most Jewish groups were the Palestinians, Israeli Bedouins, and Druze in addition to the Southern Europeans.