Index                     

Symptoms, Prognosis, and Onset

 

Symptoms

          The most recognizable symptom of the disorder is failure of puberty.  In some cases, initial failure of puberty can, later, result in a delayed or abbreviated puberty.  It can also lead to puberty with adverse or reduced effects.  Anosmia, a complete lack of smell, is an uncommon and severe symptom that could be a product of the disease in later stages.  Cryptorchidism is the absence of one or both of a scrotum’s testes, it occurs in rare cases of males with Kallmann Syndrome.  In extremely rare cases, bimanual synkinesis, simultaneous movement of both hands, can be a symptom.  That symptom is becoming obsolete, as its effects are being counteracted by medical drugs and strenuous treatment.

Onset and Prognosis

          In most cases, Kallmann Syndrome is a congenital disorder, a birth defect that primarily begins to reveal itself in early pubescent years.  Hormone treatment is a sufficient treatment option for most people diagnosed with Kallmann Syndrome.  It’s able to reverse delayed puberty and hypogonadism, a defect of the reproductive system.  Hypogonadism describes a lack of function of the gonads; ovaries in females and testes in male.

http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=3249&Disease_Disease_Search_diseaseGroup=kallmann&Disease_Disease_Search_diseaseType=Pat&Disease(s)%20concerned=Kallmann-syndrome&title=Kallmann-syndrome&search=Disease_Search_Simple

http://www.wrongdiagnosis.com/b/brachytelephalangy_characteristic_facies_kallmann/intro.htm

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http://www.kallmanns.org/node/95

On occasion, people with Kallmann Syndrome have been reported to have longer fingers and shortened metacarpal on their hands.