Lip pseudocleft-hemangiomatous branchial cyst syndrome

Introduction: Lip pseudocleft-hemangiomatous branchial cyst syndrome

Description of Lip pseudocleft-hemangiomatous branchial cyst syndrome

Lip pseudocleft-hemangiomatous branchial cyst syndrome (medical condition): A rare genetic disorder characterized by branchial defects, tear duct...more »

See also:

Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and:
  »Introduction: Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and
  »Symptoms of Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and

Lip pseudocleft-hemangiomatous branchial cyst syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Lip pseudocleft-hemangiomatous branchial cyst syndrome:

• Branchial cyst
• Lip
• Lip symptoms (1017 causes)
• Lip pain (8 causes)
• Branchial
• Cyst (86 causes)

Lip pseudocleft-hemangiomatous branchial cyst syndrome: Rare Disease

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

Lip pseudocleft-hemangiomatous branchial cyst syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Lip pseudocleft-hemangiomatous branchial cyst syndrome, or a subtype of Lip pseudocleft-hemangiomatous branchial cyst syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Lip pseudocleft-hemangiomatous branchial cyst syndrome as a Disease

Lip pseudocleft-hemangiomatous branchial cyst syndrome: Another name for Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and (or close medical condition association).
  »Introduction: Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and
  »Symptoms of Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and

Lip pseudocleft-hemangiomatous branchial cyst syndrome: Related Diseases

Lip pseudocleft-hemangiomatous branchial cyst syndrome: Lip pseudocleft-hemangiomatous branchial cyst syndrome is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Growth conditions
• Head conditions
• Oral conditions
• Congenital conditions - physical defects
• Congenital conditions

Symptoms of Lip pseudocleft-hemangiomatous branchial cyst syndrome (Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and)

Some of the symptoms of Lip pseudocleft-hemangiomatous branchial cyst syndrome incude:

• Mental retardation
• Retarded fetal growth
• Retarded growth after birth
• Low birth weight
• Atrophic branchial skin lesion

See full list of 31 symptoms of Lip pseudocleft-hemangiomatous branchial cyst syndrome (Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and)

Terms associated with Lip pseudocleft-hemangiomatous branchial cyst syndrome:

Terms Similar to Lip pseudocleft-hemangiomatous branchial cyst syndrome:

• Lee Root Fenske syndrome
• BOF syndrome
• Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
• Branchiooculofacial syndrome
• Hemangiomatous branchial clefts-lip pseudocleft syndrome

Source - NIH

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