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Since this is such a rare disorder, there is only a few people who look into it. Dr. Michael Bober is one of the few who know about this. He is an important figure when it comes to dealing with RCDP. His number to contact him is (302) 651 4000.

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Families usually have a hard time coping with this disorder mostly because when their family is diagnosed, there is no chance of escaping from or curing this disease.

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https://www.ncbi.nlm.nih.gov/books/NBK1270/               http://www.geneticdisordersuk.org/gduknetwork/rhizomelicchondrodysplasiapunctata

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THE current research of RCDP was held in a conference center where all doctors and scientists who researched this disorder come together to figure it out. The last conference was held on July 15-17, 2016

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There are a few ways to manage RCDP. Families usually have nutritionists to suggest alternatives and make diets for them. Also many kids with RCDP are not strong enough to support themselves and usually have equipment to manage their daily lives.

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Treatment for RCDP is shortened due to its rarity and comes down to just physical therapy. This treatment  helps prevent respiratory complications and also provides cognitive stimulation. Also sufferers have tendencies to overheat and usually have to be treated with temperature monitors.

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RCDP is inherited by  an autosomal recessive state, which means that it is passed down through families. The proband, or someone used as the starting point for a genetic study, has a 25% of being affected, or a 50% chance of not being affected.

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The diagnosis methods doctors use are based on clinical findings confirmed by molecular genetic testing that identifies changes in the host's chromosomes. RCDP type 1 is usually diagnosed or recognized during a neonatal period which is the time of birth to one month

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There are many symptoms from RCDP. For example, many people diagnosed usually have respiratory problems and severe intellectual disability. Also, there are chances to get seizures, hearing amplification, or cataracts.

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The discovery of RCDP isn't as complex as it would seem. For example, when doctors first discovered the disorder, they had noticed that they hadn't seen growth in the bones and had noticed cataracts in the patients eyes. This later led to the discovery of RCDP which is more deeply known as rhizomhelic chondrodysplasia punctata.