Glossary for Tooth eruption delayed
Medical terms related to Tooth eruption delayed or mentioned in this section include:
- Albers-Schonberg disease -- malignant recessive form: A rare disorder characterized primarily by increased bone density as old bone is not resorbed and replaced with new bone - is also known as marble bone disease. The malignant infantile form is the most severe form of this disorder and death usually occurs in the first decade of life.
- Breath symptoms: Breath-related symptoms including breath odor
- Breathing symptoms: Symptoms affecting the breathing systems.
- Child health symptoms: Symptoms related to pediatric (child) health.
- Cleidocranial dysplasia: A rare genetic disorder characterized by collarbone defects, late ossification of cranial sutures and delayed tooth eruption.
- Coffin syndrome 1: A rare inherited syndrome characterized mainly by spasticity, seizures, congenital heart defects, short stature and delayed mental and motor development.
- Congenital conditions: Any condition that you are born with such as birth defects or genetic diseases.
- Congenital hypothyroidism: A condition in infancy or early childhood due to an in-utero deficiency of thyroid hormones that can be caused by genetic or environmental factors, such as thyroid dysgenesis or hypothyroidism in infants of mothers treated with thiouracil during pregnancy.
- Cornelia de Lange Syndrome: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. The severity of symptoms is variable.
- Dental conditions: Conditions that affect ones dentition
- Dental symptoms: Symptoms affecting teeth or mouth area.
- Developmental problems: Physical or mental development difficulty.
- Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
- Face symptoms: Symptoms affecting the face
- Frontometaphyseal dysplasia: A rare genetic disorder characterized by craniofacial abnormalities, skeletal abnormalities, hearing problems and wasting of arm and leg muscles.
- Gaucher Disease: A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3.
- Gum disorders: Any disorder the affects the gums of the human mouth
- Head symptoms: Symptoms affecting the head or brain
- Infant symptoms: Symptoms affecting babies and infants.
- Intellectual impairment: The impairment of ones cognition
- Intrauterine infections: Infection of the fetus while still inside the womb. The type and severity of symptoms is determined by the type of infection and at what stage of pregnancy it occurs. Some cases are mild enough to be asymptomatic and others are severe enough to cause a miscarriage.
- Malnutrition: Any disorder that relates to inadequate intake of nutrients.
- Mouth symptoms: Symptoms of the mouth or oral area.
- Oculodental syndrome: A familial disorder characterized by corneal dystrophy, enlarged gums and missing teeth
- Respiratory symptoms: Symptoms affecting the breathing systems.
- Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
- Throat symptoms: Symptoms affecting the throat
- Tooth pain: Toothache due to infectious or non-infectious etiology.
- Trichorhinophalangeal syndrome type 1: A rare genetic disorder characterized by bulbous nose, sparse hair and coning of epiphyses.
- Trichorhinophalangeal syndrome type 3: A rare inherited disorder involving hair, face, teeth, and bone abnormalities. The type and severity of symptoms is variable.
- Wyburn Mason's syndrome: A rare genetic condition mainly involving enlarged brain blood vessels and skin and eye abnormalities.
Conditions listing medical symptoms: Tooth eruption delayed:
The following list of conditions
have 'Tooth eruption delayed' or similar
listed as a symptom in our database.
This computer-generated list may be inaccurate or incomplete.
Always seek prompt professional medical advice about the cause
of any symptom.
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