UNIQUE – Rare Chromosome Disorder Support Group
About UNIQUE – Rare Chromosome Disorder Support Group
The UNIQUE – The Rare Chromosome Disorder Support Group is a non-profit, voluntary organization dedicated to promoting awareness of rare chromosomal abnormalities. The organization was founded in 1984 and served as a source of support and information for anyone affected by any rare chromosome abnormality. UNIQUE acts as an international support group; produces a newsletter for registered members; and promotes awareness of rare chromosomal abnormalities, both among the public and relevant professionals. It maintains a database holding the karyotypes, phenotypes and natural histories of all affected members.
Related Rare Diseases:
- MEF2C Deficiency
- Trastorno asociado a ASXL3
- Tetrasomía 9p
- Triploidía
- Síndrome de Cri du Chat
- Síndrome ADNP
- Síndrome Dup15q
- Trisomy 9p (Multiple Variants)
- 47, XXX (Trisomy X)
- Chromosome 21 Ring
- Ring Chromosome 4
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Chromosome 18 Ring
- Chromosome 14 Ring
- Chromosome 9 Ring
- Chromosome 6 Ring
- XYY Syndrome
- Chromosome 4q Deletion
- Pallister Killian Mosaic Syndrome
- Trisomy 13 Syndrome
- Síndrome CTNNB1
- Chromosome 9, Partial Monosomy 9p
- Síndrome de anomalías congénitas múltiples asociado al gen KAT6B
- Síndrome del ojo de gato
- Síndrome de Phelan-McDermid
- Trisomía 9 en mosaico
- Trastorno relacionado a HNRNPU
- Síndrome de Jacobsen (monosomía parcial 11q)
- Trisomía 22 en mosaico
- Síndrome KAT6A
- Síndrome 48,XXYY
- Trisomía 18
- Pentasomía X
- Síndrome del cromosoma 22q en anillo