Pneumocystis Smear
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Adenovirus, Viral Culture
Amoebic Serology
Melatonin
c-KIT Mutation Analysis, Blood
Acid Sphingomyelinase Activity
Tryptase
Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
Porphobilinogen, Urine

PPOX Gene Mutation Analysis, Tissue
Medical Test

Access to PPOX Gene Mutation Analysis, Tissue is restricted.