Larsons' Homeo - Megalocornea Mental Retardation Syndrome


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Megalocornea Mental Retardation Syndrome

Treatment No. :	RD0476
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:	Aurum met 1M+d150 Corpus Vitreum D4+40C Cortisone D200+200C Gelsemium D200+200C Merc sol D200+200C Osmium D30+30C Physostigma D30+30C Rhododendron D30+30C Spigelia D200+200C Streptococcinum D200+200C
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:

Megalocornea-Mental Retardation Syndrome is an extremely rare genetic disorder characterized by distinctive abnormalities of the eyes, diminished muscle tone that is apparent at birth (congenital hypotonia), and varying degrees of mental retardation. In some cases, additional abnormalities may also be present. The range and severity of symptoms and physical findings may vary from case to case.

In most infants with Megalocornea-Mental Retardation Syndrome, the front, clear portion of the eyes through which light passes may be abnormally large (megalocornea). Both eyes are usually affected (bilateral involvement). Many affected infants also have additional eye (ocular) abnormalities including underdevelopment of the colored portion of the eyes (iris hypoplasia), abnormal "unsteadiness" of the irises during eye movements (iridodonesis), and/or other ocular abnormalities, potentially leading to varying degrees of visual impairment. In addition to abnormally diminished muscle tone (hypotonia), most affected infants also have additional neuromuscular abnormalities including abnormal delays in the acquisition of skills requiring the coordination of mental and muscular activities (psychomotor retardation) and/or an impaired ability to coordinate voluntary movements (ataxia). In most cases, affected infants and children also have moderate to severe mental retardation.

In some cases, infants and children with Megalocornea-Mental Retardation Syndrome may have additional abnormalities including short stature; episodes of uncontrolled electrical disturbances in the brain (seizures); and/or certain distinctive abnormalities of the head and facial (craniofacial) area. Such craniofacial malformations may include an unusually prominent forehead (frontal bossing), widely spaced eyes (ocular hypertelorism), a long upper lip, an abnormally small lower jaw (hypoplastic mandible), and/or unusually large and/or "cup-shaped" ears. In most cases, Megalocornea-Mental Retardation Syndrome appears to occur randomly for unknown reasons (sporadically). In other cases, the disorder is thought to be inherited as an autosomal recessive genetic trait.

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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden