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Dictionary » Chromosome 10, Trisomy 10q2
 

Chromosome 10, Trisomy 10q2

Introduction: Chromosome 10, Trisomy 10q2

Description of Chromosome 10, Trisomy 10q2

Chromosome 10, Trisomy 10q2 (medical condition): A rare chromosomal disorder where the distal portion of the long arm of chromosome 10 is duplicated so there is three copies of it instead of the normal two. The condition is characterized by drooping upper eyelid, short palpebral fissures and camptodactyly.

See also:

Chromosome 10, distal trisomy 10q:
  »Introduction: Chromosome 10, distal trisomy 10q
  »Symptoms of Chromosome 10, distal trisomy 10q

Chromosome 10, Trisomy 10q2: Related Topics

These medical condition or symptom topics may be relevant to medical information for Chromosome 10, Trisomy 10q2:

Chromosome 10, Trisomy 10q2: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Chromosome 10, Trisomy 10q2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 10, Trisomy 10q2, or a subtype of Chromosome 10, Trisomy 10q2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 10, Trisomy 10q2 as a Disease

Chromosome 10, Trisomy 10q2: Another name for Chromosome 10, distal trisomy 10q (or close medical condition association).
  »Introduction: Chromosome 10, distal trisomy 10q
  »Symptoms of Chromosome 10, distal trisomy 10q

Symptoms of Chromosome 10, Trisomy 10q2 (Chromosome 10, distal trisomy 10q)

Some of the symptoms of Chromosome 10, Trisomy 10q2 incude:

See full list of 27 symptoms of Chromosome 10, Trisomy 10q2 (Chromosome 10, distal trisomy 10q)

Chromosome 10, Trisomy 10q2: Related Disease Topics

These medical disease topics may be related to Chromosome 10, Trisomy 10q2:

Terms associated with Chromosome 10, Trisomy 10q2:

Terms Similar to Chromosome 10, Trisomy 10q2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Diaphragmatic hernia without mention of obstruction or gangrene
  • Diaphragmatic hernia, abnormal face, and distal limb anomalies
  • Diaphragmatic hernia, congenital
  • Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness
  • Diaphragmatic hernia-exomphalos-hypertelorism syndrome
  • Diaphragmatic ligament of the mesonephros
  • Diaphragmatic myocardial infarction
  • Diaphragmatic pacemaker
  • Diaphragmatic paralysis
  • Diaphragmatic part of parietal pleura
  • Diaphragmatic peritonitis
  • Diaphragmatic pleura
  • Diaphragmatic pleurisy
  • Diaphragmatic surface (of heart, liver, lung, spleen)
  • Diaphragmatic surface of heart

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