Glossary for Malformed ears in children
Medical terms related to Malformed ears in children or mentioned in this section include:
- 2-Hydroxyglutaricaciduria: A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than others.
- Ampola syndrome: A rare genetic disease characterized primarily by mental retardation, facial anomalies, short stature, seizures and finger and toe abnormalities.
- Beckwith-Wiedemann Syndrome: An inherited disorder marked by gigantism, exomphalos and macroglossia. Also called EMG syndrome and exophthalmos-macroglossia-gigantism syndrome.
- Cardiocranial syndrome: A rare syndrome characterized mainly by heart and skull abnormalities.
- Cerebrorenodigital syndrome: A rare group of syndromes characterized mainly by brain, kidney, finger and toe abnormalities.
- Child health symptoms: Symptoms related to pediatric (child) health.
- 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.
- Costello syndrome: A rare genetic disorder characterized by papillomas which may become malignant.
- Deformity symptoms: Various types of deformity
- Developmental problems: Physical or mental development difficulty.
- Ear symptoms: Symptoms affecting the ear or hearing
- Edwards Syndrome: A rare inherited genetic disorder where a portion of chromosome 18 is duplicated. Most affected individuals die during the fetal stage and surviving infants have serious defects and tend to live for only a short while.
- Face symptoms: Symptoms affecting the face
- Fibrochondrogenesis: A rare genetic disorder characterized by short stature, abnormal bone formation and stillbirth or neonatal death.
- Fuhrmann syndrome: A rare syndrome characterized mainly by abnormalities involving the thighbone, fingers and fibula (calf bone).
- Hand symptoms: Symptoms affecting the hand
- Head symptoms: Symptoms affecting the head or brain
- Leprechaunism: A very rare genetic disorder characterized by insulin resistance which leads to growth delay and endocrine system abnormalities.
- Limb symptoms: Symptoms affecting the limbs
- Malformed ears: Malformed ears are ears that are deformed.
- Potter syndrome: A congenital condition involving absence of kidneys resulting in decreased amniotic fluid and compression of the fetus. The affected baby has leg deformities, poorly developed lungs and a wrinkled, flattened facial appearance and often don't survive.
- Respiratory symptoms: Symptoms affecting the breathing systems.
- Rubinstein-Taybi Syndrome: A rare congenital disorder characterized by very small stature, broad thumbs and toes, slanted palpebral fissures and hypoplastic maxilla.
- Ruvalcaba syndrome: A very rare disorder characterized by short stature, skeletal abnormalities, mental retardation and distinctive facial features.
- Seckle syndrome: A rare genetic disorder characterized by short stature, microcephaly and a prominent nose.
- Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
- Smith-Lemli-Opitz Syndrome: A rare genetic condition involving a severe defect in the process of cholesterol synthesis resulting in low cholesterol levels in cells but high levels of the chemicals that are made into cholesterol.
- Treacher-Collins Syndrome: A rare genetic disorder characterized by malar hypoplasia, down-slanting palpebral fissures, defect of lower eye lid and malformation of external ear.
- Turner Syndrome: Rare chromosome syndrome with one X but no second X or Y chromosome.
Conditions listing medical symptoms: Malformed ears in children:
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