Glossary for Loss of teeth in children
Medical terms related to Loss of teeth in children or mentioned in this section include:
- Achondroplasia: A rare disease characterized by abnormal bone growth which results in short stature with short arms and legs, large head and characteristic facial features.
- Amelogenesis Imperfecta: An inherited dental disorder where the tooth enamel is so thin and soft that the teeth appear yellow and are easily damaged. Can occur in baby and permanent teeth. Also called hereditary brown enamel or hereditary enamel.
- Bd syndrome: A very rare syndrome characterized mainly by the association of mental retardation, small eyes and a movement disorder.
- Breath symptoms: Breath-related symptoms including breath odor
- Breathing symptoms: Symptoms affecting the breathing systems.
- Child health symptoms: Symptoms related to pediatric (child) health.
- Congenitally missing teeth in children:
- Crouzon Syndrome: A condition which is characterized by craniofacial dysostosis
- Dental symptoms: Symptoms affecting teeth or mouth area.
- Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
- Ectodermal dysplasia: A group of rare inherited conditions which affect the ectodermal skin layer which includes the skin, hair, teeth and nails.
- Ehlers danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
- Ehlers-Danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
- Face symptoms: Symptoms affecting the face
- Grief or loss: The normal emotional response that occurs to an external loss
- Hallermann-Streiff Syndrome: A condition which affects stature, head shape and hair growth
- Hay-Wells Syndrome: A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate.
- Head symptoms: Symptoms affecting the head or brain
- Incontinentia Pigmenti: A rare genetic skin pigmentation disorder characterized by eye, teeth, bone, nail and hair malformations as well as central nervous abnormalities and mental deficiency.
- Limb symptoms: Symptoms affecting the limbs
- Mouth symptoms: Symptoms of the mouth or oral area.
- Progeria: A rare fatal genetic disorder characterized by extremely premature aging.
- Respiratory symptoms: Symptoms affecting the breathing systems.
- Rieger Syndrome: A rare genetic disorder characterized by underdeveloped or absent teeth and craniofacial and eye abnormalities.
- Seckel syndrome: A rare condition characterized by fetal and postnatal growth retardation, mental retardation and characteristic facial features.
- Teeth pain: Toothache due to infectious or non-infectious etiology.
- Throat symptoms: Symptoms affecting the throat
- Van der Woude syndrome: A syndrome which is characterised by multiple congenital abnormalities
- Witkop syndrome: A syndrome that is characterised by the occurrence of nail dysplasia and tooth abnormalities due to a mutation in the MSX1 gene
Conditions listing medical symptoms: Loss of teeth in children:
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