Beckwith-Wiedemann syndrome
Protein Immunofixation Electrophoresis, Urine
Spinocerebellar Ataxia Type 3 (SCA3) (Machado-Joseph Disease) Gene Mutation Analysis
Syphilis, congenital
Vitamin B5 (Pantothenic Acid), Serum
Lactose Tolerance Test
Peritoneal effusion
Aspartate Aminotransferase (AST)
MYH7 Gene Mutation Analysis
Chlorpheniramine, Urine

Biopsy, Stomach (Gastric)
Medical Test

Access to Biopsy, Stomach (Gastric) is restricted.