Funding for Neonatal Diminosis Genetic Testing

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Information about Neonatal Diminosis is detailed
at

Diabetes Bubble / Diabetes Bubble Burst
https://prohuman.net/diabetesbubblediabetesbubbleburst.htm

...

Neonatal Diminosis
Causality / Treatment / Risk Profile

Causality / Treatment

Neonatal Diminosis should be suspected when a
High Glucose Condition is detected in the first 6
months after birth. 50% of Neonatal Diminosis is
permanent and 50% is transient, going away within
the first 18 months of age

The treatment is based on the specific gene causing
the condition, as depicted in the following tables.

[see link above for those details]

...

It occurs in from 1 in 100,000 to 1 in 500,000 births.

The permanent forms of Neonatal Diminosis are similar
to other Diminosis conditions (the exception being their
occurrence within 6 months after birth), but the transient
forms are unique in that, like Gestational Cellosis, they
go away but can recur.

It may be treated with sulfonylureas, although exogenous
insulin may be required.

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The following article solicits funding for a genetic testing
program for 500 children with Neonatal Diminosis:
https://www.inyourarea.co.uk/news/help-fund-lifesaving-research-programme-for-babies-with-diabetes/

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o 11 specific types of Diminosis (new name
created in 2010 for a monogenic condition
> age 6 months that sometimes is called
maturity onset diabetes of the young, some-
times confusingly called diabetes with no
clarifier), unpreventable & non-reversible
(thus far).

o 12 specific types of Neonatal Diminosis
(new name created in 2010 for a monogenic
condition at age < or = 6 months that some-
times is called neonatal diabetes, sometimes
confusingly called diabetes with no ...

... clarifier), 8 types are permanent & unpre-
ventable & nonreversible (thus far); 4 specific
types are transient but can recur.

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