Abstract
The urofacial syndrome, also known as Ochoa syndrome, is a rare autosomal recessive condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems due to a dysfunctional bladder. We report 11 patients with urofacial syndrome in five families from Turkey with a median follow up of 32 months (range, 2-44 months).
MeSH terms
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Abnormalities, Multiple
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Antibiotic Prophylaxis / methods
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Catheterization / methods
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Child
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Cholinergic Antagonists / therapeutic use
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Combined Modality Therapy
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Face / abnormalities*
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Facial Expression
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Follow-Up Studies
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Humans
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Male
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Syndrome
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Urinary Bladder, Neurogenic / complications*
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Urinary Bladder, Neurogenic / therapy
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Urinary Incontinence / complications*
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Urinary Incontinence / therapy
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Urinary Tract Infections / complications*
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Urinary Tract Infections / therapy
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Vesico-Ureteral Reflux / complications*
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Vesico-Ureteral Reflux / therapy