The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. If available, the list includes a rough estimate of how common a feature is (its frequency). Frequencies are based on a specific study and may not be representative of all studies. You can use the MedlinePlus Medical Dictionary for definitions of the terms below.
|Signs and Symptoms||Approximate number of patients (when available)|
|Abnormality of the teeth||90%|
|Coarse facial features||90%|
|Everted lower lip vermilion||90%|
|Prominent supraorbital ridges||90%|
|Thick lower lip vermilion||90%|
|Broad nasal tip||-|
|Exaggerated median tongue furrow||-|
|Heavy supraorbital ridges||-|
|Maxillary lateral incisor microdontia||-|
|Prominent median palatal raphe||-|
|Widely-spaced maxillary central incisors||-|
|X-linked dominant inheritance||-|
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.