Larsons' Homeo - Ablepharon Macrostomia Syndrome


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Ablepharon Macrostomia Syndrome

Treatment No. :	RD0011
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:	Baryta Carb D25+100C Calc Phos D25+100C Iodium D25+100C Medorrhinum D100+100C Psorinum D100+100C Thuja D25+100C
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 :	30 ml Drops
Order Online:	One 30 ml bottle for $79.99 Two 30 ml bottles for $129.99

Condition Overview:

Ablepharon-Macrostomia Syndrome (AMS) is an extremely rare inherited disorder characterized by various physical abnormalities affecting the head and facial (craniofacial) area, the skin, the fingers, and the genitals. In addition, affected individuals may have malformations of the nipples and the abdominal wall. Infants and children with AMS may also experience delays in language development and, in some cases, mental retardation.

In infants with Ablepharon-Macrostomia Syndrome, characteristic craniofacial features may include absence or severe underdevelopment of the upper and lower eyelids (ablepharon or microblepharon) as well as absence of eyelashes and eyebrows; an unusually wide, "fish-like" mouth (macrostomia); and/or incompletely developed (rudimentary), low-set ears (pinnae). Abnormalities of the eyes may occur due to, or in association with, ablepharon or microblepharon. Individuals with AMS may also have additional characteristic features including abnormally sparse, thin hair; thin, wrinkled skin with excess (redundant) folds; webbed fingers with limited extension; and/or malformations of the external genitals. In some cases, additional features associated with AMS may include absent or abnormally small (hypoplastic) nipples and/or abdominal wall abnormalities. Although the exact cause of Ablepharon-Macrostomia Syndrome is not fully understood, some cases suggest that the disorder may be inherited as an autosomal recessive genetic trait.
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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden