Acid maltase deficiency

Acid maltase deficiency

Acid maltase deficiency (AMD), also known as Pompe disease, is a genetically inherited disease that affects muscle function. Inherited diseases are passed on from parents to a child.

Acid maltase deficiency
By Paul A. JohnsonThe Gale Group Inc., Gale.. Gale Encyclopedia of Genetic Disorders Part I, 2002more »
Definition ...

Acid maltase deficiency
Alpha-1,4-glucosidase acid deficiency
GSD type 2
Pompe disease
Type 2 glycogenosis ...

Acid Maltase Deficiency
TDC
Taurodeoxycholic Acid; Thermal Dilution Catheter; Time-density Curve [computed Tomography]; Total Dietary Calories ...

Acid Maltase Deficiency
Alpha-1,4 Glucosidase Deficiency
Cardiomegalia Glycogenica Diffusa
Generalized Glycogenosis
Glycogenosis Type II
Lysosomal Glucosidase Deficiency ...

Acid Maltase Deficiency
Carnitine Deficiency
Carnitine Palmityl Transferase Deficiency ...

Acid Maltase Deficiency
Acidemia, Isovaleric
Acidemia, Methylmalonic
Acidemia, Propionic
ACL (Anterior Cruciate Ligament) Injuries
ACL (Anterior Cruciate Ligament) Injury, Physical Therapy for
ACL (Anterior Cruciate Ligament) Surgery ...

Acid Maltase Deficiency see Pompe disease
Acne
Acne Vulgaris see Acne
Acoustic Neuroma
Acquired Aplastic Anaemia
Acquired Aplastic Anemia see Acquired Aplastic Anaemia
Acquired Haemochromatosis see Haemochromatosis ...

Type II (Pompes disease, acid maltase deficiency)
Type III (Coris disease, debrancher enzyme deficiency)
Type IV (Andersens disease, brancher enzyme deficiency)
Type V (McArdles disease, muscle glycogen phosphorylase deficiency) ...

Type II (Pompe's disease, acid maltase deficiency)
Type III (Cori's disease, debrancher enzyme deficiency)
Type IV (Andersen's disease, brancher enzyme deficiency)
Type V (McArdle's disease, muscle glycogen phosphorylase deficiency) ...

Type II (Pompe's disease, acid maltase deficiency)
Type III (Cori's disease, debrancher enzyme deficiency)
Type IV (Andersen's disease, brancher enzyme deficiency)
Type V (McArdle's disease, muscle glycogen phosphorylase deficiency) ...

Synonym(s): Neurological Manifestations of Pompe Disease, Acid Maltase Deficiency, Glycogen Storage Disease
Table of Contents (click to jump to sections) ...

Protein Chlamydomonas, Hospital, City, Hydralazine Hydrochloride, Infections, Nosocomial, Kinases, Protein-Serine-Threonine, Library Technical Services, Myxofibromas, Neoplastic Pregnancy Complications, Nystagmus, Positional, Acid Maltase Deficiency ...

Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency, Schindler Type
Lysosomal Glucosidase Deficiency
Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency
Lysosomal Storage Disorders
Lyssa ...

See also: Deficiency, Symptom, Storage disease, Glycogen Storage Disease, Weakness