Sterling silver Trisomy 21 necklace, representing the extra copy of chromosome 21 in Down Syndrome.
Close-up of trisomy 21 Down Syndrome necklace on a model, showing its sleek and elegant design.
Down Syndrome-inspired necklace featuring three copies of chromosome 21, crafted in silver.

trisomy 21 - Down syndrome necklace

silver
|

€ 160

Length

45 cm + 5 cm extender chain included

Choose your extra chain

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Trisomy 21 necklace | sterling silver

If you teach chromosome 21 to medical students, you are also teaching Alzheimer's biology. The APP gene sits on chromosome 21. People with Down syndrome carry an extra copy, and their risk of early-onset Alzheimer's is dramatically elevated. Jérôme Lejeune discovered the extra chromosome in 1959, opening the entire field of cytogenetics.

The Science Behind Trisomy 21

Trisomy 21 is caused by three copies of chromosome 21, occurring in approximately 1 in 700 live births. Jérôme Lejeune identified the extra chromosome in 1959 in Paris, establishing the chromosomal basis of Down syndrome. The amyloid precursor protein (APP) gene sits on chromosome 21, and the gene dosage imbalance results in APP overexpression. This connection makes Down syndrome a natural genetic model for Alzheimer's disease: people with Down syndrome develop Alzheimer's pathology earlier and more consistently than the general population. Research linking Down syndrome and Alzheimer's biology has advanced understanding of amyloid processing relevant to broader neurodegenerative disease. Life expectancy has risen from approximately 25 years in the 1980s to around 60 years with modern medical care.

The Audience

  • genetic counselors and clinical geneticists specialising in chromosomal disorders
  • Alzheimer's researchers and neurodegenerative disease specialists
  • families, caregivers, and advocates for people with Down syndrome
  • researchers in prenatal medicine and chromosomal biology

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FAQ

Is this a meaningful gift for someone working in genetic counselling?

Yes. Trisomy 21 is one of the most important chromosomal diagnoses in medical genetics. Genetic counselors, clinical geneticists, and researchers working on Down syndrome or Alzheimer's biology all carry this knowledge as core to their work. A pendant that holds the third chromosome acknowledges that weight.

Why is chromosome 21 so significant for Alzheimer's research?

Because the APP gene on chromosome 21 is responsible for producing amyloid-beta when imbalanced. People with Down syndrome carry an extra copy, leading to consistent APP overexpression and early Alzheimer's pathology. This makes Down syndrome a unique natural model for studying amyloid-driven neurodegeneration, offering insights that have advanced treatment approaches for the broader Alzheimer's population.

What size, material, and chain?

19 mm pendant in 925 polished sterling silver, nickel-free and hypoallergenic. 45 cm sterling silver chain with 5 cm extender. Ships free worldwide via DHL Express in 1-5 business days. Comes in a ready-to-gift eco-friendly box with the 30-day “Love It or Return It” policy.

How does this pendant relate to other chromosomal pieces in the catalog?

The trisomy 21 pendant is the chromosomal-disorder piece. The DNA necklaces (H and V) are the molecular-structure pieces, useful for general genetics audiences. Mendel's peas marks classical genetics. The four together span the discipline from inheritance to chromosomes to molecular structure. Many genetics labs collect across the family.

Genetics

Our genetics-inspired jewelry captures the essence of life's code in striking detail. Crafted to mirror the DNA double helix, each piece is more than an aesthetic marvel—it's a tribute to the complexity of our genetic makeup. Far from ordinary, this collection combines scientific precision with artistic flair, making each item a captivating blend of form and function. It's not just an accessory; it's a meaningful representation of the miracle that is genetics.

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