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Menkes Disease With Daniel DeFabio From Global Genes

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Manage episode 432191167 series 3485028
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Nicknamed Kinky Hair Syndrome Menkes Syndrome is tested for in cases where the child isn't getting enough copper which can cause hair loss. It is often the first sign. It isn't on the newborn screening currently, but their are clinical trials for it. Go to clinicaltrials.gov for more information if your child has it. Babies won't show signs often until it is to late.
Daniel has a background in video editing and animation and has worked on shows like The Closer and Curb Your Enthusiasm. Today he works at Global Genes and uses his skills to help rare disease patients tell their story through film.
I am currently trying to turn Rare Connection into a nonprofit. I am looking for volunteer board members to help with that. It is a volunteer position, so you won't be paid, but it is a good way to gain experience and help the rare disease community. Please contact me through the link in the fan mail link in the show notes if interested. Also please subscribe wherever you are seeing this Thanks for listening.

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28 episodes

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Manage episode 432191167 series 3485028
Content provided by Joanna. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joanna or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Send us a Text Message.

Nicknamed Kinky Hair Syndrome Menkes Syndrome is tested for in cases where the child isn't getting enough copper which can cause hair loss. It is often the first sign. It isn't on the newborn screening currently, but their are clinical trials for it. Go to clinicaltrials.gov for more information if your child has it. Babies won't show signs often until it is to late.
Daniel has a background in video editing and animation and has worked on shows like The Closer and Curb Your Enthusiasm. Today he works at Global Genes and uses his skills to help rare disease patients tell their story through film.
I am currently trying to turn Rare Connection into a nonprofit. I am looking for volunteer board members to help with that. It is a volunteer position, so you won't be paid, but it is a good way to gain experience and help the rare disease community. Please contact me through the link in the fan mail link in the show notes if interested. Also please subscribe wherever you are seeing this Thanks for listening.

Support the Show.

  continue reading

28 episodes

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