Otopalatodigital syndrome type 1 is a disorder mostly entailing irregularities in skeletal advancement. It is a member of a group of associated conditions called otopalatodigital spectrum disorders, which additionally consists of otopalatodigital syndrome type 2, frontometaphyseal dysplasia, Melnick-Needles syndrome, and terminal bony dysplasia. Otopalatodigital syndrome type 1 is usually the mildest of the otopalatodigital spectrum disorders. Affected individuals additionally have hearing loss. Babies with otopalatodigital syndrome type 1 may be birthed with an opening in the roof of the mouth. Individuals with this problem often have less teeth than normal. People with otopalatodigital syndrome type 1 might be somewhat shorter than other members of their family. Females with otopalatodigital syndrome type 1 typically have more variable symptoms and signs contrasted to affected men, with females normally having fewer signs and symptoms.
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