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Urinary, reproductive, and developmental conditions

1,521 articles

Bohring-Opitz syndrome

Bohring-Opitz syndrome (BOS, Oberklaid-Danks syndrome) is a rare ASXL1-related autosomal dominant disorder with IUGR, trigonocephaly, BOS posture, severe intellectual disability, and Wilms tumor screening needs.

Bowen-Conradi syndrome

Bowen-Conradi syndrome (Bowen Hutterite syndrome, BWCNS) is a lethal autosomal recessive ribosomopathy caused by an EMG1 D86G mutation, common in Hutterites (1/355 births), with microcephaly, contractures, and death in infancy.

Brachydactyly

Brachydactyly: short fingers or toes from abnormal phalange, metacarpal, or metatarsal development. Types A-E (Bell classification); types A3 and D affect about 2% of people; genes include IHH, ROR2, GDF5, HOXD13.

Brachydactyly type B

Brachydactyly type B (BDB) is a rare congenital condition in which the ends of the fingers, but not the thumbs, are underdeveloped or absent, with missing fingernails.

Branchio-oculo-facial syndrome

Branchio-oculo-facial syndrome (BOFS) is a rare autosomal dominant disorder caused by TFAP2A mutations, marked by neck skin defects, eye malformations, cleft lip, and hearing loss.

Branchioskeletogenital syndrome

Branchioskeletogenital syndrome, also called Elsahy-Waters syndrome or BSG syndrome, is an ultra-rare CDH11-related congenital malformation syndrome with craniofacial, dental, vertebral, and genital anomalies, moderate intellectual disability, and about 7 reported cases.

Breast abscess

Breast abscess, also called mammary or puerperal abscess (ICD-11 GB21.0), is a localized pus collection in the breast, usually complicating mastitis; treated by aspiration or incision and drainage with antibiotics, nonlactational forms recur in 25-57%.

Breast cancer

Breast cancer, cancer arising in breast duct or lobule cells, is the most common cancer in women and leading cause of female cancer death; 2.43 million new cases in 2024, five-year survival over 90% in high-income countries versus about 40% in South Africa.

Breast disease

Breast disease is any condition affecting the breast, spanning malignant conditions, chiefly breast cancer, and benign inflammatory, fibroepithelial, and hormonal disorders; evaluation typically uses triple assessment.

Breast hypertrophy

Breast hypertrophy (macromastia, gigantomastia) is excessive benign breast tissue growth in females, defined by over 5 pounds or 3% body weight excess, treated with medication or reduction surgery.

Breech birth

Breech birth, also called breech presentation, is delivery of a baby buttocks- or feet-first, occurring in 3–4% of term births; managed by external cephalic version, planned cesarean, or selected planned vaginal breech birth.

BRESEK syndrome

BRESEK syndrome, also called BRESHECK syndrome (OMIM 308205), is an extremely rare X-linked multiple congenital malformation syndrome caused by MBTPS2 mutations, combining brain anomalies, severe intellectual disability, ectodermal dysplasia, skeletal, ear/eye, and kidney defects; all reported patients are male.

Bright's disease

Bright's disease (morbus Brightii), a historical term named for Richard Bright, covered proteinuric kidney disease from his 1827 Reports of Medical Cases until renal biopsy replaced it with glomerulonephritis and modern diagnoses in the 1950s.

Brooke Greenberg

Brooke Greenberg (1993–2013), Maryland woman with unexplained "syndrome X" developmental arrest; at 20 had infant size, toddler mind; genome sequenced by Mount Sinai; distinct from progeria.

Buried penis

Buried penis, also called concealed or hidden penis, is a normal-sized penis covered by prepubic skin or fat. Covers congenital and adult acquired forms, causes such as obesity and lichen sclerosis, and surgical outcomes.

C syndrome

C syndrome, or Opitz trigonocephaly syndrome (OMIM 211750), is a rare congenital malformation syndrome with trigonocephaly from metopic synostosis, intellectual disability, hypotonia, cardiac defects, and CD96 or IFT140 involvement.

C10orf53

C10orf53 (chromosome 10 open reading frame 53, HGNC:27421) is a human protein-coding gene at 10q11.23 encoding the uncharacterized 93-aa UPF0728 protein Q8N6V4; testis-enriched, spermatid expression, GWAS links to glaucoma and prostate carcinoma.

Calculus in bladder

Calculus in bladder (bladder stone, vesical calculus): hard mineral mass forming in the urinary bladder, usually from incomplete emptying; classified primary, secondary, or migratory; treated by cystolithotripsy.

Calculus in urethra

A calculus in the urethra, also called urethrolithiasis, is a urinary stone lodged in the tube that carries urine from the bladder, usually presenting as acute urinary retention.

Calculus of kidney

Calculus of kidney (renal stone, ICD-11 GB70.0): a mineral concretion in the renal collecting system, mostly calcium-based, diagnosed by non-contrast CT, treated with NSAIDs, SWL, URS, or PCNL, and recurrent in up to 39% at 15 years.

Calculus of lower urinary tract

Calculus of lower urinary tract (ICD-11 GB71): stones in the bladder or urethra, also called vesical or urethral calculi; bladder stones are about 5% of urinary stones, mostly secondary to bladder outlet obstruction, treated by transurethral cystolithotripsy.

Calculus of prostate

Calculus of prostate (prostatic calculi, prostatolithiasis, ICD-11 GA91.3): small calcium carbonate or calcium phosphate calcifications forming in the prostate, common in men over 50, usually asymptomatic, not independent predictors of severe LUTS.

Calculus of upper urinary tract

Calculus of upper urinary tract (ICD-11 GB70) covers kidney and ureteral stones, mostly calcium oxalate. Key facts: 106 million 2021 incident cases, 45% ultrasound sensitivity, PCNL for stones over 2 cm.

Calculus of ureter

Calculus of ureter (ureterolithiasis, ureteric stone; ICD-10-CM N20.1, ICD-11 GB70.1) is a urinary stone, usually formed in the kidney, lodged in the ureter, causing renal colic; passage rates and treatment depend on stone size and location.

Candida balanoposthitis

Candida balanoposthitis, also called candidal balanitis, is Candida albicans infection inflaming the glans penis and foreskin of uncircumcised men; treated with clotrimazole or miconazole cream, linked to diabetes and older age.

Carcinoma in situ of bladder

Bladder carcinoma in situ (CIS, stage 0is/Tis): flat, always high-grade, noninvasive urothelial cancer of the bladder lining; primary, concomitant, or secondary; ~54% progress untreated; treated with BCG or cystectomy.

Carcinoma in situ of breast

Carcinoma in situ of the breast (DCIS, LCIS; stage 0 breast cancer, intraductal carcinoma): noninvasive lesions confined to breast ducts or lobules; 15–25% of diagnoses, over 98% five-year survival, central overdiagnosis and active surveillance debate.

Carcinoma in situ of endometrium

Carcinoma in situ of endometrium (ICD-11 2E67.0, ICD-10-CM D07.0): abnormal cancer-like cells confined to the uterine lining without invasion; covers the legacy term for endometrial precancer (AH/EIN) and serous endometrial intraepithelial carcinoma.

Carcinoma in situ of penis

Carcinoma in situ of the penis, also called penile intraepithelial neoplasia grade III, erythroplasia of Queyrat (glans), or Bowen's disease (shaft), is a noninvasive full-thickness squamous atypia, HPV-related, with up to 30% untreated progression risk.

Carcinoma in situ of vagina

Carcinoma in situ of vagina, also called VaIN 3 or vaginal HSIL, is a full-thickness noninvasive HPV-associated precancerous vaginal lesion, rare (0.2–2 per 100,000 women yearly), treated by laser, excision, brachytherapy, or topical agents.