Larsons' Homeo - Chromosome 9, Trisomy 9p (Multiple Variants)


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Chromosome 9, Trisomy 9p (Multiple Variants)

Treatment No. :	RD0313
Dosage & Instructions:	30 drops in water after meal.
Composition:	Absinthium D3 Artemisia vulg D2 Collinsonia canad D3 Nux vomica D4 Lupulinum D2 Mentha piperita TM Acorus calamus TM
Treatment Type:	This remedy is a symptomatic treatment. A symptomatic treatment cannot eliminate the disease from its root but is able to considerably improve the patient's condition by easing his or her symptoms.
Contra-indications:	None established
Special Instructions:	Whereas this remedy can be safely used by teenagers, its use has not been evaluated in children under 12 years of age. Please do not administer to children under this age.
Storage:	Store in a cool and dry place
Precautions:	Keep away from the reach of children
Standard Packaging :	90 ml Drops
Order Online:	One 90 ml bottle for $79.99 Two 90 ml bottles for $129.99

Condition Overview:

This disease entry was made possible due to the generosity of the Robert Lee and Clara Guthrie Patterson Trust, through grant funds provided for the National Organization for Rare Disorders' "Pediatric Rare Disease Database Project."

Chromosome 9, Trisomy 9p is a rare chromosomal syndrome in which a portion of the 9th chromosome appears three times (trisomy) rather than twice in cells of the body. The trisomy may involve a portion of the short arm (9p), the entire short arm, or the short arm and a portion of the long arm (9q) of chromosome 9. (Each chromosome contains a short arm known as "p" and a long arm designated as "q.") Evidence suggests that, in many cases, associated symptoms and findings may be relatively similar among affected infants despite differing lengths of the trisomic (duplicated) segment of 9p. However, in those with larger trisomies (e.g., extending to middle or end [distal] regions of 9q), additional features may also be present that appear to correlate with the extent of the duplication.

Virtually all individuals with Trisomy 9p are affected by mental retardation and distinctive malformations of the skull and facial (craniofacial) region. In some instances, additional physical abnormalities may also be present, such as other skeletal defects, structural malformations of the heart that are present at birth (congenital heart defects), and/or other findings. In some cases, the trisomy appears to result from a balanced chromosomal rearrangement in one of the parents; in others, it is thought to arise from spontaneous (de novo) errors very early in embryonic development that occur for unknown reasons (sporadically).

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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden