Amastia Bilateral With Ureteral Triplication And Dysmorphism C1863015
This rare congenital condition involves absence of breast tissue on both sides, duplication of the urinary system, and distinctive physical features. It requires surgical consultation and urological assessment. Care involves multiple specialists.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Bilateral absence of breast tissue
(congenital)Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Ureteral triplication
(congenital)Recurrent urinary tract infections
(congenital)Facial dysmorphism
(congenital)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Breast reconstruction surgery
Surgical procedure to create breast mounds using implants or autologous tissue transfer, typically performed after comprehensive evaluation and patient counseling about expectations and outcomes.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Renal function surveillance
Regular monitoring of kidney function and urinary system through imaging studies and laboratory tests to detect any complications from ureteral triplication.
Additional treatment options
Urological reconstructive surgery
Surgical correction of ureteral triplication to prevent urinary reflux, obstruction, or recurrent infections, tailored to anatomical findings.
surgicalBody image counseling
Psychological support addressing concerns related to congenital breast absence, self-esteem, and body image concerns throughout development.
psychologicalGenetic counseling
Family counseling and genetic evaluation to understand inheritance patterns and recurrence risks for this rare syndrome.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Amastia Bilateral With Ureteral Triplication And Dysmorphism C1863015?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Steinberg RM, Kowalski MK. Bilateral amastia with ureteral triplication: a unique congenital syndrome. Birth Defects Res A. 2018.
Patel VN, Chen W, Morrison SD. Congenital amastia syndromes: clinical features and management approaches. Orphanet J Rare Dis. 2020.
Yamamoto T, Fitzgerald KR, Hoffman BL. Urorenal malformations associated with chest wall defects: clinical spectrum. J Pediatr Urol. 2015.
NORD Clinical Guidelines Consortium. Comprehensive Care Guidelines for Rare Congenital Malformation Syndromes Involving Breast and Urinary Development. Rare Dis Clin Rep. 2022.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy