A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects

Introduction: A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects

Description of A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects (medical condition): A rare disorder characterized by destruction of ends of finger bones, mental retardation, skin wasting and eye and facial abnormalities.

See also:

Van Bogaert-Hozay syndrome:
  »Introduction: Van Bogaert-Hozay syndrome
  »Symptoms of Van Bogaert-Hozay syndrome

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects: Related Topics

These medical condition or symptom topics may be relevant to medical information for A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects:

• Mild mental retardation
• Acro-osteolysis
• Mental retardation (1917 causes)
• Skin atrophy (32 causes)
• Facial dysmorphism
• Familial
• Form
• Acro
• Osteolysis
• Mental

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects, or a subtype of A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects as a Disease

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects: Another name for Van Bogaert-Hozay syndrome (or close medical condition association).
  »Introduction: Van Bogaert-Hozay syndrome
  »Symptoms of Van Bogaert-Hozay syndrome

Symptoms of A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects (Van Bogaert-Hozay syndrome)

Some of the symptoms of A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects incude:

• Mental retardation
• Concentration difficulties
• Learning difficulties
• Facial abnormalities
• Atrophic skin

See full list of 27 symptoms of A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects (Van Bogaert-Hozay syndrome)

A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects: Related Disease Topics

These medical disease topics may be related to A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects:

• hypertelorism
• micrognathia
• malocclusion
• arched palate
• hypoplasia of cilia and eyebrows
• eyelid ptosis
• alternating squint
• astigmatism and myopia
• mental retardation

Terms associated with A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects:

Terms Similar to A Familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects:

• Acro-osteolysis-facial dysplasia syndrome
• Hozay’s syndrome
• Van Bogaert-Hozay syndrome

Source - NIH

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