OTHER GENETIC AND CHROMOSOMAL ANOMALIES

Testo italiano di questa pagina

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(**) Italian translation provided / con versione italiana

*Tuberous sclerosis, in a child with epilepsy, autism and mental retardation; Report of the rehabilitative and drug therapy intervention (**)

* First months of drug therapy in a Cri-du-chat case (**)

* Drug therapy in a girl aged ten with Smith-Magenis syndrome (last updating, Februaru 2008 ) (**)

* Drug therapy in Aicardi-Goutieres syndrome: Report of a 61-months folloup (last updating: October 2004) (**)

* Twenty-seven months of antistress drug therapy in a girl with partial trisomy 22. (Updated up to 51 months) (**)

* A second case with Smith-Magenis syndrome treated primarily with antistress drug therapy lasting five months (**)

* Twenty-seven months of antistress drug therapy in a girl with partial trisomy 22. (updated to 97 months of treatment) (**)

* Fifteen months of palliative therapy, even with manganese sulfate, in two siblings with neural-axonal dystrophy of Hallervorden-Spatz (updating June 2003).

* Treatment with antistress drugs of a GM1 gangliosidosis, of probable intermediate juvenile-adult type. (updated, April 2004 (**).

 * Therapy with antistress drugs on phenotypic symptoms in a child with particular chromosomal anomalies ( unbalanced translocation 16-17 and partial trisomy 17). (Updated March 2006) (**)

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