Abdominal muscle syndrome

Brief introduction of abdominal muscle deficiency syndrome Orbinsky Syndrome is a dysplasia of the abdominal muscles, often associated with abnormalities in organs such as the extremities, urinary tract, gastrointestinal tract, and heart. The main clinical manifestations are that the abdominal wall is as thin as paper, the organs inside the abdomen are faintly visible, and the touch by hand is clearer. If the patient does not use the arm force, the patient cannot be transferred from the lying position to the sitting position. Abdominal pressure is insufficient when coughing, and there are often respiratory infections. The skin at the lower part of the rib is red. The incomplete type of abdominal wall is normal, showing only bilateral cryptorchidism and urinary malformations. basic knowledge The proportion of illness: 0.003% Susceptible people: no special people Mode of infection: non-infectious complication:

Absence of abdominal muscle deficiency syndrome

Abdominal muscle dysplasia, abdominal muscle weakness, often cause respiratory and urinary system infections. The incomplete type of abdominal wall is normal, showing only bilateral cryptorchidism and urinary malformations.

Abdominal muscle deficiency syndrome prevention

Mainly to prevent respiratory infections and urinary tract infections.

Complications of abdominal abscess syndrome Complication

Respiratory infections, urinary malformations, gastrointestinal and cardiac malformations.

Abdominal muscle deficiency syndrome symptoms Common symptoms Abdominal muscle developmental oliguria Renal failure Congenital abdominal wall hypoplasia

The main clinical manifestations are that the abdominal wall is as thin as paper, the intra-abdominal organs are faintly visible, and the touch by hand is clearer. If the patient does not use the arm force, the patient cannot be changed from the lying position to the sitting position. When the cough is insufficient, the abdominal pressure is insufficient, and the respiratory tract infection is often present. The skin is red, and the incomplete type of abdominal wall is normal, showing only bilateral cryptorchidism and urinary malformations.

Urinary malformations can be expressed as:

1 complete urethral obstruction, renal failure after birth, urinary surgery drainage still oliguria, short-term death from uremia.

2 severe upper urinary tract structure and functional damage, uremia progresses rapidly, for acute kidney or ureteral stoma drainage, the ureter is obviously dilated and lacks peristalsis.

3 urinary tract obstruction is mild, the symptoms in childhood are not serious, can be corrected by surgery, but the conservative treatment failure rate is 80%.

Examination of abdominal abscess syndrome

Generally need to do B-ultrasound, CT, abdominal plain film and other imaging examinations.

Diagnosis and differentiation of abdominal muscle deficiency syndrome

Can be diagnosed based on clinical performance and laboratory tests.

Urinary stones, influenza, glomerulonephritis, etc.

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