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Symptoms » Pointy chin » Glossary
 

Glossary for Pointy chin

Medical terms related to Pointy chin or mentioned in this section include:

  • 3-M Syndrome: A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected.
  • Alagille syndrome: A genetic disorder affecting the liver and characterized by the absence of some or all of the liver bile ducts that transport bile within the liver.
  • Bone symptoms: Symptoms affecting the body's bones
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Chin symptoms: Symptoms affecting the chin
  • Chromosome 2 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 2 instead of the normal two.
  • Chromosome 22q13 deletion: A very rare chromosomal disorder where a portion of chromosome 22 is missing at the q13 location which results in various abnormalities.
  • Chromosome 4, trisomy 4q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 4 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 4q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 4 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Davenport-Donlan syndrome: A very rare syndrome characterized mainly by deafness, white hair, contractures and papillomas.
  • Del (3) (q12-q21): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in a few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Deletion 22q13: A very rare chromosomal disorder where a portion of chromosome 22 is missing at the q13 location which results in various abnormalities.
  • Developmental problems: Physical or mental development difficulty.
  • Dup (2) (pter-p23): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Face symptoms: Symptoms affecting the face
  • Gloomy syndrome: A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected.
  • Harrod Doman Keele syndrome: A very rare syndrome characterized mainly by skull, facial, genital, finger and toe abnormalities.
  • Head symptoms: Symptoms affecting the head or brain
  • Infant symptoms: Symptoms affecting babies and infants.
  • Jaw symptoms: Symptoms affecting the jaw
  • Megarbane-Jalkh Syndrome: A rare condition reported in two related infants and involving a range of abnormalities such as developmental delay, unusual facial features, wrinkled skin, liver failure and fragile bones. One of the infants died before the age of 2 years due to liver failure.
  • Mental retardation, X-linked -- hypotonia -- facial dysmorphism -- aggressive behavior: A rare X-linked disorder characterized by mental retardation, reduced muscle tone, aggressive behavior and unusual facial appearance. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
  • Mental retardation, X-linked, 59: A rare form of mental retardation inherited in a X-linked manner. It occurs as a result of a defect in the sigma-2 subunit of the adaptor protein-1 gene on chromosome Xp22. Mental retardation ranged from mild to severe.
  • Mental retardation, X-linked, 93: A rare form of mental retardation inherited in a X-linked manner. It occurs as a result of a defect in the BRWD3 gene. Female carriers may also suffer from some mental deficiency.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Multiple pterygium syndrome: A very rare disorder characterized by webbing of various parts of the body, contractures, short stature, fusion of neck vertebrae and facial anomalies.
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Nasopalpebral lipoma -- coloboma syndrome: A very rare syndrome characterized mainly by a hole in the eyelids, telecanthus and fat deposits (lipomas) on the nose and eyelids.
  • Osteodysplasia, familial, Anderson type: A very rare syndrome characterized mainly by skeletal abnormalities involving the spine, legs, pelvis and collar bone.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Skull symptoms: Symptoms affecting the skull surrounding the brain.
  • Soto's Syndrome: A rare hereditary disorder characterized by excessive growth during the first few years of life as well as various other mental and physical anomalies.
  • Stargardt Macular Degeneration, Absent or Hypoplastic Corpus Callosum, Mental Retardation and Dysmorphic Features: A rare syndrome characterized by the association of eye and brain abnormalities, mental retardation and a distinctive facial appearance.
  • Throat symptoms: Symptoms affecting the throat
  • Trigonocephaly -- ptosis -- mental retardation: A very rare syndrome characterized mainly by droopy eyelids, mental retardation and a triangular shaped forehead.
  • Unusual facies, arachnodactyly, hypogenitalism and failure to thrive: A very rare syndrome characterized by an unusual facial appearance, small genitals, failure to thrive and long, thin fingers.
  • Zellweger-like syndrome, without peroxisomal anomalies: A rare syndrome characterized by unusual facial appearance, very low muscle tone, mental retardation and metabolic defects.

Conditions listing medical symptoms: Pointy chin:

The following list of conditions have 'Pointy chin' 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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