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Gorlin-Chaudhry-Moss syndrome: MedlinePlus Genetics

    https://medlineplus.gov/genetics/condition/gorlin-chaudhry-moss-syndrome/
    In individuals with an SLC25A24 gene mutation, Gorlin-Chaudhry-Moss syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.In these cases, the condition results from new …

Gorlin-Chaudhry-Moss Syndrome - National …

    https://rarediseases.org/rare-diseases/gorlin-chaudhry-moss-syndrome/
    In Gorlin-Chaudhry-Moss syndrome, premature closure of the fibrous joints (coronal sutures) between bones in the front (frontal bone) and sides (parietal bones) of …

Gorlin Chaudhry Moss syndrome - About the Disease

    https://rarediseases.info.nih.gov/diseases/66/gorlin-chaudhry-moss-syndrome/
    About Gorlin Chaudhry Moss syndrome. Many rare diseases have limited information. Currently GARD is able to provide the following information for Gorlin Chaudhry Moss …

About: Gorlin-Chaudhry-Moss syndrome - North Carolina …

    https://rarediseases.oscar.ncsu.edu/disease/gorlin-chaudhry-moss-syndrome/about/
    Gorlin-Chaudhry-Moss syndrome is a condition that affects many parts of the body. The signs and symptoms of this disorder are apparent from birth or infancy. Gorlin-Chaudhry …

Gorlin-Chaudhry-Moss syndrome - MedlinePlus

    https://medlineplus.gov/download/genetics/condition/gorlin-chaudhry-moss-syndrome.pdf
    Some individuals with Gorlin-Chaudhry-Moss syndrome have mild developmental delay but intelligence is usually normal in this disorder, as is life expectancy. Frequency Gorlin …

Orphanet: Gorlin Chaudhry Moss syndrome

    https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=2095
    Gorlin-Chaudhry-Moss (GCM) syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysostosis, facial dysmorphism, conductive hearing loss, …

Gorlin-Chaudhry-Moss Syndrome | Hereditary Ocular Diseases

    https://disorders.eyes.arizona.edu/disorders/gorlin-chaudhry-moss-syndrome
    Systemic Features: Premature closure of the coronal suture and midface hypoplasia lead to striking brachycephaly. The scalp hairline is low and scalp hair is abundant and coarse. In …

Gorlin Chaudhry Moss Syndrome - DoveMed

    https://www.dovemed.com/diseases-conditions/gorlin-chaudhry-moss-syndrome/
    Gorlin Chaudhry Moss syndrome is an extremely infrequent congenital condition that may be manifest in an autosomal recessive manner. Typically, in …

Gorlin-Chaudhry-Moss syndrome - North Carolina State University

    https://rarediseases.oscar.ncsu.edu/disease/gorlin-chaudhry-moss-syndrome/
    Also known as: craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence; craniofacial …

Gorlin-Chaudhry-Moss syndrome - Medical Dictionary

    https://medical-dictionary.thefreedictionary.com/Gorlin-Chaudhry-Moss+syndrome
    Gorlin-Chaudhry-Moss syndrome: ( gōr'lin chaw'drē mos ), [MIM*233500] craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, and …



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