The following Conditions are related to Cleft lip

Select a specific condition below to view its details.

  • Ectodermal dysplasias

    Each of the nearly 100 EDs has its own set of clinical signs and symptoms. Commonly, the conditions will have one or more of the following associated findings: Teeth: reduced number, abnormal shape or size Hair: abnormal structure, sparse, slow-growing, often light-colored Sweat glands: often reduced number and abnormal structure, leading to decreased sweat production and risk of elevated body temperature (hy  Read More

  • Faciogenitopopliteal syndrome

    IRF6-related disorders include a spectrum of disorders caused by abnormalities in the interferon regulatory factor 6 (IRF6) gene. Van der Woude syndrome (VWS) is at the mild end of the spectrum and popliteal pterygium syndrome (PPS) is at the severe end of the spectrum. Individuals with VWS can have lip pits alone, cleft lip or cleft palate alone, or a combination of these anomalies.The physical features associated with PPS include  Read More

  • Hay-wells syndrome

    Hay-wells syndrome, also termed Ankyloblepharon-ectodermal dysplasia-cleft lip/palate (AEC) syndrome, is a rare autosomal inherited disorder that occurs due to the changes in the TP63 gene.There is no cure for the syndrome. Certain treatment plans are implemented to manage the symptoms and prevent complications in the affected individuals. It includes,Antibiotics – People with this syndrome will b  Read More

  • Rapp hodgkin syndrome

    Rapp-Hodgkin syndrome is a rare disease that is caused by a defect in genes. It can cause problems to hair, nails, skin, teeth, and sweat glands. The child may inherit one faulty gene from each parent and resulting in this syndrome.The child with Rapp-Hodgkin syndrome may have opened in the upper lip, skin erosions, fused eyelids, growth problems, hair loss, and other problems associated with appearance. him99999 U  Read More

  • Ws -- waardenburg syndrome

    Waardenburg syndrome (WS) is a group of genetic disorders named after Dutch ophthalmologist and geneticist Petrus Johannes Waardenburg, who described it. This is an autosomal dominant inherited disorder. This rare disease results in the loss of pigmentary cells in the eyes, skin, stria vascularis of the cochlea, and hair.This type of disease may cause features like facial abnormalities like the diminished coloratio  Read More