Ovotestis is a hermaphroditic gonad, with both testicular and ovarian tissue. The term Ovotestis is coined up from ovary and testis. While Ovotestis is a normal feature in some animals such as gastropod Helix aspersa, it is an anatomical abnormality in humans associated with gonadal dysgenesis. A hermaphroditic reproductive organ that can produce both sperm and eggs, is found in certain gastropods. Less than 20% of people with true hermaphroditism are diagnosed before 5 years of age and about 75% are diagnosed by age 20. True hermaphroditism is a genetically heterogeneous condition caused by certain phenotypic, gonadal and molecular theoretical factors.
In such gonads the ovaries occupy normal abdominal position although sometimes they may be found at the internal inguinal ring. Many patients with true hermaphroditism have a uterus and internal duct development corresponding to the adjacent gonad. In approximately 50% of Ovotestis, there is evidence of ovulation.
Persons with true hermaphroditism have ambiguous genitalia at birth. The majority are reared as males due to the size of the phallus. However, due to the functioning of normal ovarian tissue, most of them experience breast development at puberty and abnormal menstruation cycles. Apart from these syndromes, there are not many other developmental abnormalities in these patients. The mortality rate is also not that alarming for affected individuals. They usually possess average intelligence.
Such true hermaphroditism is a rare condition and they are less than 10% of intersex cases. More than 400 such cases have been reported worldwide. Interestingly geographical variation have been noted and the highest occurrence of such cases is found in the Southern African population.
After childbirth, the usual and much awaited announcement from a midwife in the labor ward is - 'it's a boy' or 'it's a girl'. But there are instances when the midwife cannot determine the sex of the baby as the sex organs do not conform to defined norms of a male or a female. The baby is born with sex organs that aren't clearly male or female. There is ambiguity about the gender. The child is born with a disorder of sex development (DSD). In all probability the midwife may relate to the newborn as 'baby'. Here is a child diagnosed with DSD at birth.
An estimated 2,000 babies are born 'intersex' each year, referring to a set of over 60 different conditions that fall under the diagnosis of 'DSD' (Differences/Disorders of Sex Development). DSD occurs more often than Down syndrome or cystic fibrosis. In the last 15 years, there is more openness about DSD which has led to moving beyond the medical/biological realm. There is growing interest in gender studies as well.
From Intersex syndrome to DSD
Other terms in place of disorder of sex development are 'intersex' (between the sexes) or 'hermaphrodite' or 'pseudohermaphroditism'. International experts held a conference (International Consensus Conference on Intersex) in 2006 and have reached a consensus that the term DSD or disorder of sex development should replace all those terms.
Some people prefer to use terms like 'differences in sex development' or 'diversity of sex development'. There are three basic types of DSDs. These manifest in different ways. Understanding X and Y chromosomes can help in sorting out the types of DSDs.
Females have two X chromosomes (XX) in each cell. This is by inheriting one X chromosome from each parent. Two X chromosomes is medically written as Karyotype 46, XX. And males have an X chromosome and a Y chromosome (XY). This is by inheriting an X chromosome from the mother and a Y chromosome from the father. An XY is referred to as Karyotype 46, XY.
The Y chromosome helps make a boy as it contains the genes for the development of male organs like the testes and penis. This happens around the 6th week of fetal development. As the testes make testosterone, the penis, scrotum and urethra form. Between 7th and 8th month of the pregnancy, the testes descend into the scrotum. In the absence of the Y chromosome, the fetal tissue in a female fetus (XX) will form the female sex organs – the ovaries, uterus and the fallopian tubes.
Causes of disorder of Sex development
Through the many stages of sex development, if all is typical the fetus develops into a normal male or a female. But, if at any stage of sex development an atypical development takes place it results in a 'disorder of sex development. Like:
Types of DSDs
Diagnostic approach to DSD
Diagnosis begins with determining the type of disorder of sex development. Physical examination, medical history of the mother's health during pregnancy and family history of any neo-natal deaths form part of the diagnosis. A biopsy of the reproductive organs is done where necessary.
Treatment of DSD
Treatment options are based on specific diagnosis and issues involved. Not restricted to medical treatment, it involves psychological support as well. Reconstructing external genitalia or removing internal genitalia are surgical procedures. In some cases, more than one surgery is needed.
Surgical procedures for DSD
Not every DSD requires surgery. Medications may also be used to treat certain DSDs. Experts recommend waiting till adolescence to understand the individual's preference for identity. In children, surgery is necessary:
Feminizing surgery: Going by 'Chicago Consensus', Feminizing surgery should only be considered in cases of severe virilisation. Also, the emphasis should be on functional outcome rather than cosmetic appearance. An ongoing debate on Feminizing Surgery is the timing of the surgery. A section believes in performing early feminizing surgery. Yet another section advocate feminizing surgery in adolescence as the patient is involved in discussions and decision-making.
Pseudohermaphroditism is the term normally employed to describe people born with secondary sexual characteristics. In this condition of sexual ambiguity, the individual pseudohermaphrodite possesses gonadal tissue of one sex but exhibits external phenotype of the opposite sex. The external sex organs in some of these people look intermediate between the typical vagina or penis. In some others, the appearance is that of an 'opposite' gonadal tissue. Due to this factor, pseudohermaphroditism is difficult to detect until puberty. This is a congenital condition.
The term 'male pseudohermaphrodite' is used when the testis is present; 'female pseudohermaphrodite' is used when the ovary is present. In pseudohermaphroditism the genital and sex determinations are discordant, for instance an apparently female individual may have testes, a male pseudohermaphrodite. Some symptoms of pseudohermaphroditism include, abnormal female external genitalia, enlarged clitoris, fusion of labia and sealed vagina.
In male pseudohermaphroditism, the individual has male chromosomal and gondal gender with female external genitalia. Male pseudohermaphroditism is a defect in the male embryo and usually a genetic deficit in androgen production or action. Accurate diagnosis and careful assessment of all clinical features is vital in treatment of pseudohermaphroditism conditions. The sex hormone binding globulin suppression test using anabolic steroid is used in confirming the diagnosis. This is performed during the neonatal period. Tests involving administration of gonadotrophic hormones are also useful in determining whether the body can produce testosterone or whether the problem involves ability to use testosterone.
Surgery is sometimes performed to alter the appearance of the genitals. The modern day approach is to delay the surgery and wait for the child to mature in order to express a preference. Hormone therapy, support and counseling are other treatment methods usually employed.Tags: #Ovotestis #DSD #Pseudohermaphroditism
Enter your health or medical queries in our Artificial Intelligence powered Application here. Our Natural Language Navigational engine knows that words form only the outer superficial layer. The real meaning of the words are deduced from the collection of words, their proximity to each other and the context.
Diseases, Symptoms, Tests and Treatment arranged in alphabetical order:
Bibliography / Reference
Collection of Pages - Last revised Date: August 13, 2022