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Imperforate Anus

108  relevant articles (0 outcomes, 9 trials/studies) found for this Disease

Description: A congenital abnormality characterized by the persistence of the anal membrane, resulting in a thin membrane covering the normal ANAL CANAL. Imperforation is not always complete and is treated by surgery in infancy. This defect is often associated with NEURAL TUBE DEFECTS; MENTAL RETARDATION; and DOWN SYNDROME.

Also Known As:
Anus, Imperforate; Anal Atresias; Atresias, Anal; Anal Atresia; Atresia, Anal

Disease Context: Research Results

Related Diseases

1. Hirschsprung Disease (Hirschsprung's Disease)
2. Constipation
3. Fistula
4. Syndrome
5. Hypospadias

Experts

1. Bonnot, O: 2 articles (11/2003 - 08/2001)
2. Robert, E: 2 articles (11/2003 - 08/2001)
3. Oshio, Takehito: 1 article (01/2008)
4. Novotny, Nathan M: 1 article (12/2007)
5. Rescorla, Frederick J: 1 article (12/2007)
6. Shelley, Anita A: 1 article (12/2007)
7. Mattix, Kelly D: 1 article (12/2007)
8. Tobias, Joseph D: 1 article (12/2007)
9. Zhengwei, Yuan: 1 article (03/2005)
10. Weilin, Wang: 1 article (03/2005)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Imperforate Anus:
1. Lorazepam (Ativan)FDA LinkGeneric
2. Complement System Proteins (Complement)IBA
3. tranilast (N 5')IBA
4. SynaptophysinIBA
5. Polyurethanes (Polyurethane)IBA
6. BenzodiazepinesIBA
7. glutamyl- glycyl- valyl- tyrosyl- valyl- histidyl- prolyl- valineIBA
8. TriadFDA Link
9. Valproic Acid (Valproate, Semisodium)FDA LinkGeneric
05/15/2008 - "These included patients with chromosomal abnormalities (25, 29.0%); non-chromosomal syndromes including Beckwith-Wiedemann syndrome, Goltz syndrome, Marshall-Smith syndrome, Meckel-Gruber syndrome, Oto-palato-digital type II syndrome, CHARGE syndrome, and fetal valproate syndrome; malformation sequences, including ectopia cordis, body stalk anomaly, exstrophy of bladder, exstrophy of cloaca, and OEIS (Omphalocele, Exstrophy of bladder, Imperforate anus, Spinal defect); malformation complexes including Pentalogy of Cantrell, and non-syndromic multiple congenital anomalies (MCA) (26, 30.2%)"
06/01/2007 - "This article provides a comprehensive review of omphalocele-related disorders: otopalatodigital syndrome type II; Melnick-Needles syndrome; Rieger syndrome; neural tube defects; Meckel syndrome; Shprintzen-Goldberg omphalocele syndrome; lethal omphalocele-cleft palate syndrome; cerebro-costo-mandibular syndrome; fetal valproate syndrome; Marshall-Smith syndrome; fibrochondrogenesis; hydrolethalus syndrome; Fryns syndrome; omphalocele, diaphragmatic defects, radial anomalies and various internal malformations; diaphragmatic defects, limb deficiencies and ossification defects of skull; Donnai-Barrow syndrome; CHARGE syndrome; Goltz syndrome; Carpenter syndrome; Toriello-Carey syndrome; familial omphalocele; Cornelia de Lange syndrome; C syndrome; Elejalde syndrome; Malpuech syndrome; cervical ribs, Sprengel anomaly, anal atresia and urethral obstruction; hydrocephalus with associated malformations; Kennerknecht syndrome; lymphedema, atrial septal defect and facial changes; and craniosynostosismental retardation syndrome of Lin and Gettig"
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10. Growth Hormone (Somatotropin)IBA

Therapies and Procedures

1. Biofeedback (Psychology) (Biofeedback)
2. Colostomy
3. Cecostomy
4. Enema (Enemas)
5. Transplants (Transplant)

Best Treatments:
Research Summary Report
on Imperforate Anus
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