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Hypospadias and epispadias are congenital defects of the urinary tract. This means they occur during intrauterine development. There is no genetic basis for the defects. Specific causes for hypospadias are not known.
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The severity of hypospadias is defined according to the distance of the urethral opening from its normal location at the tip of the penis.
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The genetic risk of hypospadias is estimated to be around 7-10%, suggesting a multifactorial etiology involving both genetic and environmental factors. Studies have shown an increased incidence of hypospadias among first-degree relatives of affected individuals, indicating a potential genetic component to the condition.
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if it is Education Core then there are chances to accept you otherwise there are a lot of chances that you will be rejected, however, the condition of Hypospadias will be observed,
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Hypospadias and epispadias are both congenital conditions of the urethra. Both conditions are more common in males, but can occur in females.
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Hypospadias
Found only in male infants; urethral orifice is located on ventral surface of penis.
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Surgery is the treatment of choice for both hypospadias and epispadias. All surgical repairs should be undertaken early and completed without delay. This minimizes psychological trauma.
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Hypospadias repair refers to a group of surgical approaches used to correct or reconstruct parts of the external genitalia and urinary tract related to a displaced meatus, or opening of the urethra.
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Use ICD-9 code 752.61 for the diagnosis of Hypospadias. And CPT code 54324 for 1-stage distal hypospadias repair for which meatal advancement is performed.
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The most common surgical technique for correcting hypospadias in girls is construction of a new urethra that opens to the outside of the body rather than emptying into the vagina. Tissue is taken from the front wall of the vagina for this purpose.
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Hyposadias is a mispelling of "hypospadias", which is an abnormal development of the external genitalia.
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Hypospadias is a congenital condition where the opening of the urethra is on the underside of the penis instead of at the tip. It typically does not affect penis size but can influence the appearance and function of the penis. Surgical correction is often needed to reposition the urethral opening to the tip of the penis.
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Epispadias is the medical term for a congenital defect in which the urethra opens on the dorsum of the penis. Epispadias is due to a defect in the tissue that folds inward to form the urethra.
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That would be very, very unusual.
A very rare condition called "hypospadias".
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you may have to do a certain position when you're having sex.
contact your ob about this.
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54322
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752.61
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Hypospadias surgery does not typically affect penis size. The goal of the surgery is to correct the position of the urethral opening and improve urinary function, not to alter the size of the penis. The size of the penis is determined by genetic factors and hormones, not by hypospadias surgery.
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Some people regard it as unnecessary interference with a child's body and a traumatic experience with psychological consequences extending into adult life.
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No, as it is not medically necessary in most cases. However, in cases of certain congenital anatomic abnormalities involving the penis (such as hypospadias) it would be covered.
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There is not enough information in the question to provide a comprehensive answer. Your best bet is to see a urologist who will examine you for any problems that may be related to the surgery to correct your hypospadias. ---- I agree. I assume you have been urinating normally, so your urethra must be working OK. You don't say whether you have an orgasm or not. If you cannot reach orgasm the problem may not be physical at all.
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It may be challenging for an adult male with untreated hypospadias and chordee to satisfy a female sexually due to difficulties with penetration and potential pain during intercourse. Seeking medical treatment can help improve sexual function and satisfaction. Communication and exploring alternative ways of intimacy can also be beneficial in maintaining a satisfying sexual relationship.
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Hypospadias -involves an abnormally placed [[urinary meatus]] (opening). Instead of opening at the tip of the [[glans penis|glans]] of the [[penis]], a hypospadic ure ... Hypospadias are among the most common birth defects of the male genitalia (second to [[cryptorchidism]]), but widely varying incidences http://en.wikipedia.org/wiki/Special:Search?search=Urinary+opening+male&go=Go
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He could have hypospadias, a condition in which the opening of the urethra is on the underside of the penis, instead of at the tip. It can be surgically corrected but as long as he has not had any infections then there is nothing to worry about.
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Male external urinary tract defects are discovered at birth during the first detailed examination of the newborn. Female urethral defects may not be discovered for some time due to the difficulty in viewing the infant vagina.
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It would depend on the woman. It is likely that they would have questions as to why it appears different than a typical penis, but when you explain it, it would be up to them as to whether they like it or not. Typically, if she likes you enough it won't matter too much.
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The normal male urethral opening is at the tip or end of the penis.
IndicationsHypospadias is a congenital anomaly in which the urethral opening is at the base of the penis, or along the inferior aspect of the shaft of the penis. Hypospadias is usually associated with an abnormal curvature of the penis, called "chordee". Hypospadias is one of the most common birth defects seen in infant boys. Surgery is necessary to allow normal urination, to correct the penis deformity, and to ensure normal sexual functioning. The repair is performed before the child reaches school age.
ProcedureSurgical repair of hypospadias is done while the child is deep asleep and pain-free (using general anesthesia). The goals of the surgery are to repair the abnormal curvature of the penis, and to create a new urethra at the tip of the penis. A small piece of foreskin can be used to create a tube to extend the urethral length to allow placement of the urethral opening at the tip of the penis. Circumcision should NOT be performed at birth so that the foreskin can be used for the repair.
AftercareThe type of repair depends on the severity of the defect. Mild defects may be repaired in a single procedure, while severe defects may require two or more procedures. Hypospadias repair is usually performed before the age of three years.
Reviewed ByReview Date: 09/19/2011
Linda J. Vorvick, MD, Medical Director, MEDEX Northwest Division of Physician Assistant Studies, University of Washington, School of Medicine; and Louis S. Liou, MD, PhD, Chief of Urology, Cambridge Health Alliance, Visiting Assistant Professor of Surgery, Harvard Medical School. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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The foreskin covers the head of the penis (glans) to protect it and keep it moist and sensitive. It is designed to retract during arousal to expose the glans for stimulation during sexual activity.
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The suffix "-spadias" refers to a condition where a body part is displaced or positioned incorrectly. It is commonly used in medical terms to describe congenital defects such as hypospadias (urethral opening on the underside of the penis) or epispadias (urethral opening on the upper side of the penis).
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They have a hole there so they can ejaculate sperm and semen and so they can pee, or go wee-wee
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Some disorders of the male reproductive system affect the penis, such as erectile dysfunction or hypospadias. Some disorders affect the testes, such as testicular cancer. Still others, like hydrocele, affect the scrotum.
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It is called phalloplasty and it is usually used for the construction or reconstruction of a penis (occasionally it is referred to as penis enlargement). The first phalloplasty was done for a sexual reassignment (the first female-to-male reassignment).
This reconstruction, or a complete construction, of a penis is usually done on:
- Males who have lost their penis for whatever reason
- People with congenital irregularities such as hypospadias, epispadias, and micropenis
- Female-to-Male transsexual people.
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This could be a condition called hypospadias, where the opening of the urethra is not at the tip of the penis. It can cause the urine stream to split into two separate streams. It is important to see a healthcare provider for proper evaluation and treatment.
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For female children of mothers who took DES during pregnancy: You have a higher risk of vaginal cancer; you have a higher risk of breast cancer; you have a higher risk of infertility; you have a higher risk of premature births; and, you have a higher risk of autoimmune diseases. For male children of mothers who took DES during pregnancy: You have a higher risk of hypospadias; you may have a higher risk of testicular cancer; and, you seem to have a higher risk to be trangendered.
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A child with Klinefelter syndrome does not usually have any prominent features. Any physical characteristics are subtle. They may have curved little fingers (clinodactyly), difiiculty straightening out the arms completely (radioulnar synostosis), an armspan that exceeds height, a depression in the chest (pectus excavatim), occasionally undescended testicles or hypospadias (urethra under the penis rather than at the tip), leg length greater than head to seat height. Children with xxy may have low muscke tone, and may have delays indevloping lnguage. Some appear to have mild autism.
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Ocular hypertelorism is a condition where there is an increased distance between the eyes, causing them to be abnormally far apart. This can be a result of underlying genetic or developmental factors and may be associated with other craniofacial abnormalities. Treatment may involve surgery to correct the positioning of the eyes.
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(2+2)/(2+2)=1
(2/2)+(2/2)=2
(2*2)-(2/2)=3
(2+2+2)-2=4
(2+2)+(2/2)=5
(2*2*2)-2=6
((2-.2)/.2)+2=7
2+2+2+2=8
(22/2)+2=9
((2+2)*2)+2=10
((2-.2)/.2)+2=11
(2+2+2)*2+=12
(22/2)+2=13
(2/.2)+(2+2)=14
2+(2/2)/.2=15
(2+2)*(2+2)=16
...??????????=17
((2+2)/.2)-2=18
((2+2)-.2)/.2=19
22- √(2+2)=20
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230.
2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2*2 = 1073741824
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- 2,222,222
- 2 + 2 + 2 + 2 + 2 + 2 + 2 = 7(2) = 14
- 2 - 2 - 2 - 2 - 2 - 2 - 2 = 2 - 6(2) = -10
- 2*2*2*2*2*2*2 = 27 = 128
- 2/2/2/2/2/2/2 = 2/26 = 1/32
Otherwise, it's just a bunch of 2's.
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256
2, 128
2, 2, 64
2, 2, 2, 32
2, 2, 2, 2, 16
2, 2, 2, 2, 2, 8
2, 2, 2, 2, 2, 2, 4
2, 2, 2, 2, 2, 2, 2, 2
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2+2+2+2+2+2+2+2+2+2+2+2+(2x0)
=2+2+2+2+2+2+2+2+2+2+2+2+0
=24
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2 * 2 * 2 * 2 * 2 * 2 * 2, or 27.
Broken down as follows.....
128
2, 64
2, 2, 32
2, 2, 2, 16
2, 2, 2, 2, 8
2, 2, 2, 2, 2, 4
2, 2, 2, 2, 2, 2, 2
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