Potentials Foundation

Registration is only for those with MOPD I/III, MOPD II, Meier-Gorlin and remarkably similar microcephalic primordial dwarfism not otherwise specified.
Entry criteria: MOPDII and other similar Microcephalic Primordial Dwarfism conditions of MOPDI/III, Meier-Gorlin, and those not otherwise specified - in absence of another existing syndrome, are based on subjective, clinical diagnosis without definitive tests. Foundation entry will be defined by the presence of certain inclusionary criteria, without the presence of 2 or more exclusionary criteria. If entry criteria are not met, families will have the option to appeal to the Medical Advisory Board on a quarterly basis. We recognize those under 2 years of age may not yet have experienced or be aware of sufficient inclusionary criteria for inclusion, and may appeal to Medical Advisory Board for review. The Potentials Foundation reserves the right to revoke registration at any time for any reason. The Potentials Foundation Board of Directors has the right to final ruling determination.

Your contact information:
Full name:
 * required
Names of parents:
 * required
Names of sibblings:
Email address:
 * required
Street address:
 * required
City:
 * required
State, Province, or Region:
 * required
Postal Code:
 * required
Country:
 * required
Telephone number:
Alternate phone number:
Add my contact info to the family directory:
Additional information:
Diagnosis:
If Other or Unknown please provide details:
Name of diagnosing physician and institution:
 * required
Have you tested for gene mutations? If so do you have the results:
Please indicate any known chromosomal changes:
Date of birth:
 * required
Birth weight:
 * required
Term:
 * required
Length at birth:
 * required
Head circumference at birth:
 * required
Current weight:
 * required
Current height:
 * required
Current head circumference:
 * required
Wingspan: the measurement from fingertip to fingertip of outstretched arms:
 * required
Wingspan measured by Doctor or Parent:
Amount of growth in the last 12 months:
 * required
Best description of childhood activity level:
Best description of your child's development:
Your child's communication method:
Vision issue requiring glasses:
Hearing loss:
Narrow airway resulting in a high pitched voice:
Vascular stenosis, moyamoya or aneurysm:
Type 2 diabetes:
Elevated cholesterol or blood lipids:
High blood pressure or kidney issues:
Scoliosis or thoracic kyphosis:
Forearm Mesomelia (disproportionately shortened):
Coxa Vara or similar hip joint dislocation issues:
Elbow dislocation or range of motion issues:
Hyperflexive ligaments:
Missing Patella:
Early Feeding Issues:
Early Respiratory Issues:
Delayed bone age:
Small teeth, reduced enamal, shallow roots:
Fine sparse hair:
Darkened skin pigmentation spots:
Shoe size:
Clothing size:
 * required
Please list any additional medical concerns:
How may we assist you:
Comments:

Registration is a two-part process.  After submitting the registration form you will receive an email request for two photos of the face; one of which should be a front view and the other should be a profile view.  Potentials Foundation Review Board verifies all submissions before access to the foundation is given.

 

 

Potentials Foundation - A Cause for Chloe 
PO Box 34
Sandoval IL 62882
USA

info@potentialsfoundation.org

Families with a MOPDI/III, MOPDII, Meier-Gorlin or remarkably similar microcephalic primordial dwarfism not otherwise specified
diagnosis are invited to CLICK HERE and register with the foundation to join the family support
We would like to refer families with other forms of Primordial Dwarfism to the following sites for support:
Seckel Syndrome http://groups.yahoo.com/group/seckel-loop/
Russell-Silver Syndrome www.magicfoundation.org/www/docs/112/russel-silver-syndrome