Autosomal Dominant Opitz G/BBB Syndrome
This genetic disorders:** known as Autosomal Dominant Opitz G/BBB Syndrome, can be Discussed here.
Persons finding themselves or loved ones distressed in their lives because of Autosomal dominant opitz G/BBB syndrome, related: 22q11.2 deletion syndrome may like to share how they cope in order to help others world-wide searching for experiences.
** A mutation / chromosome / missing or additional gene(s)
Control mechanism unveiled for gene that causes Opitz syndrome. Opitz G/BBB (Opitz) syndrome is a hereditary disorder that affects people in different ways, causing malformations in medial (Midline) organs and structures, intellectual disability and developmental disorders. Scientists have revealed a new control mechanism for the gene that causes this disorder, a discovery that could help in developing treatment for the syndrome. The findings were published on May 16 in the online edition of Development. Ref. Source 1z.