Kallmann(KAL1) and Steroid Sulphatase Deficiency(STS) Probe Combination Probe

FMDC-20

Kallmann syndrome (KS)is a developmental disorder characterised by olfactory deficiency and hypogonadotrophic hypogonadism (HH), which is responsible for the absence of spontaneous puberty.
Steroid Sulphatase Deficiency (STS) (also known as X-linked Ichthyosis) is the second most common type of ichthyosis, and one of the most frequent human enzyme deficiency disorders.

5 Tests, 10 Tests

Red/Green

Human

Xp

For Research Use Only. Not for use in diagnostic procedures.

Store at minus 20 centigrade

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