Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Dictionary » CAH, isolated 17,20-lyase deficiency
 

CAH, isolated 17,20-lyase deficiency

Introduction: CAH, isolated 17,20-lyase deficiency

Description of CAH, isolated 17,20-lyase deficiency

CAH, isolated 17,20-lyase deficiency (medical condition): A form of congenital adrenal hyperplasia where a...more »

See also:

17-20 desmolase deficiency:
  »Introduction: 17-20 desmolase deficiency
  »Symptoms of 17-20 desmolase deficiency

CAH, isolated 17,20-lyase deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for CAH, isolated 17,20-lyase deficiency:

CAH, isolated 17,20-lyase deficiency as a Disease

CAH, isolated 17,20-lyase deficiency: Another name for 17-20 desmolase deficiency (or close medical condition association).
  »Introduction: 17-20 desmolase deficiency
  »Symptoms of 17-20 desmolase deficiency

CAH, isolated 17,20-lyase deficiency: Related Diseases

CAH, isolated 17,20-lyase deficiency: CAH, isolated 17,20-lyase deficiency is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of CAH, isolated 17,20-lyase deficiency (17-20 desmolase deficiency)

Some of the symptoms of CAH, isolated 17,20-lyase deficiency incude:

  • Ambiguous male external genitalia
  • Males with female external genitalia
  • Absence of menstruation
  • Failure to develop secondary sex characteristics
  • Reduced testosterone level

CAH, isolated 17,20-lyase deficiency: Related Disease Topics

These medical disease topics may be related to CAH, isolated 17,20-lyase deficiency:

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Congenital lymphedema
  • Congenital macroglossia
  • Congenital macular changes
  • Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
  • Congenital malaria
  • Congenital malformation
  • Congenital MD
  • Congenital megacolon
  • Congenital megalo-ureter
  • Congenital melanocytosis with myelomeningocele and hydrocephalus

    Find out more

    Search to find out more about CAH, isolated 17,20-lyase deficiency:

      
      
    powered by
    Google
  •  

    By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

    Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise