DGSX

Introduction: DGSX

Description of DGSX

DGSX (medical condition): A rare genetic disorder characterized by accelerated growth, a peculiar face...more »

See also:

Simpson-Golabi-Behmel syndrome, type 1 (SGBS1):
  »Introduction: Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)
  »Symptoms of Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)

DGSX as a Disease

DGSX: Another name for Simpson-Golabi-Behmel syndrome, type 1 (SGBS1) (or close medical condition association).
  »Introduction: Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)
  »Symptoms of Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)

DGSX: Related Diseases

DGSX: DGSX is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Growth conditions
• Congenital conditions - physical defects
• Congenital conditions
• Fetal health conditions
• Mental retardation conditions
• Intellectual or developmental disabilities

Symptoms of DGSX (Simpson-Golabi-Behmel syndrome, type 1 (SGBS1))

Some of the symptoms of DGSX incude:

• Increased birth weight
• Mental retardation
• Reduced muscle tone
• Prenatal accelerated growth
• Postnatal accelerated growth

See full list of 47 symptoms of DGSX (Simpson-Golabi-Behmel syndrome, type 1 (SGBS1))

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