Autism associations

Regarding genetic and developmental syndromes

Today I took some hours to look at associated genetic developmental syndromes. I looked at studies from 2004 to the present , they were easy to find, there have been a lot of studies done which mention autism as associated to these syndromes, some of which are quite rare. If there was any question that autism is developmental or genetic in origin, perhaps this will be informative.

Search any of these scientifically and medically defined syndromes by name and add “autism” to the search key words for as much information as you can handle. The studies are there in significant numbers.

List from this morning’s work. Any diagnosis can be “stand alone” or it can be “co morbid”, these seem to be associated with autism often enough to have been mentioned in over 24 studies I used to compile these associated syndromes. I am sure there will be more if I continue the search and study. Do you have, or do you know anybody who has one or more of these syndromes and is/are also autistic?

Names of Genetic Syndromes associated with autism

Hamartoma
Fragile X

Cri-duChat

Tuberous Sclerosis Rett

Down

Phenylketonuria

CHARGE

Angelman
Prader Willi
Neurofibromatosis
Laurence Moon Bidel
Joubert
Goldenhar
Hypomelanosis of Ito
Noonan
Sotos
VCF
Lebers amaurosis
Ehle rDanlos
Williams
Ludan Fryns
Coffin Lowrey
Moebius
ADNP
Cohen
HEADD
Phelan Mcdermid
Stenert
Timothy
Marinesaro Sjodgren
Smith Lenli Opitz
Coffin Siris
Duchennes
2Q deletion
De Lange
Rubenstien Taybi
MOMO
Smith Magenis
Apert

All of these syndromes involve genetic changes that cause differences in development of various parts and systems of the body. Interesting, Isn’t it?







2 thoughts on “Autism associations

  1. There are people on the spectrum in both maternal and paternal sides of my family. Ehlers Danlos syndrome is also present in both sides of my family. It really makes sense that these syndromes are found together. Ehlers Danlos is a collagen and connective tissue disorder; but somehow it is also related to thiamine deficiency and dietary oxalate sensitivity.
    It’s like “gene packages” ( groups of comorbid genes) run in families.

    Liked by 1 person

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