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Try out PMC Labs and tell us what you think. Learn More. Pentasomy 49,XXXXY is a rare sex chromosome disorder usually presenting with ambigous genitalia, facial dysmorphism, mental retardation and a combination of cardiac, skeletal and other malformations. The incidence of the condition is estimated to be 1 in 85, male births. ly, this condition was identified as a Klinefelter variant. The condition is suspected in a patient, by a combination of characteristic clinical findings, and the diagnosis is confirmed by chromosome culture and karyotyping.

In the case we report here, the main presentation of ambiguous genitalia led to a suspicion of a sex chromosome aneuploidy which was subsequently confirmed by chromosomal analysis. Pentasomy 49,XXXXY is a rare sex chromosome polysomy, clinically expressed as a combination of mental retardation, facial dysmorphism, genital, cardiac, and skeletal malformations. A baby boy who was noticed to have ambiguous genitalia at birth was referred for genetic studies.

He was the first baby born to a non-consanguineous couple a year-old woman and a year-old man. The pregnancy had been uneventful till delivery. The baby has been delivered at 38 weeks of gestation by lower segment cesarean section due to the head not being engaged.

The birth weight was 2. The child had developed head control by the age of 3 months and showed social smile at 10 weeks of age. The other examination findings were: brachycephaly, mild upward slant of the eyes, flat nasal bridge, bilateral clinodactyly and micropenis Both testis were in well formed scrotal sacs. The urethral opening was at the normal position on the tip of the penis.

Ultrasound scan of the abdomen showed bilateral hydroceles. Although initially 49,XXXXY pentasomy was considered a variant of Klinefelter syndrome, it is currently recognized as a separate clinical entity distinguished by facial features, multiple skeletal and cardiac defects and short stature. This produces a secondary oocyte with four X chromosomes, which, when fertilized by a Y chromosome bearing sperm, in an embryo with 49,XXXXY syndrome.

Characteristic clinical features of 49,XXXXY syndrome are the triad of mental retardation, radioulnar synostosis, and hypogonadism. There are a range of other associated phenotypic features such as low birth weight, slow growth with retarded bone age, craniofacial anomalies, abnormal genitals, widely spaced nipples, cardiac deformities, and skeletal abnormalities. Facial dysmorphism is characterized by a full round face, hypertelorism, telecanthus, and upslanted palpebral fissures.

In this case, the genital abnormalities were the main features which led to a suspicion of a sex chromosome aneuploidy that was confirmed by chromosomal analysis. There are reports of the condition diagnosed in babies presenting with genital abnormalities at birth. The prognosis of these children depends on the extent girls for sex near me severity of the condition while the management mandates a multidisciplinary approach with pediatric endocrinology, pediatric surgery, orthopedics, psychiatry, and clinical genetic evaluations.

Source of Support: Nil. Conflict of Interest: None declared. National Center for Biotechnology InformationU. Indian J Hum Genet. Vajira H. Dissanayake1, 2 Palinda Bandarage1 Christeen R. Pedurupillay2 and Rohan W. Jayasekara 1. Christeen R. Rohan W. Author information Copyright and information Disclaimer.

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Abstract Pentasomy 49,XXXXY is a rare sex chromosome disorder usually presenting with ambigous genitalia, facial dysmorphism, mental retardation and a combination of cardiac, skeletal and other malformations. Introduction Pentasomy 49,XXXXY is a rare sex chromosome polysomy, clinically expressed as a combination of mental retardation, facial dysmorphism, genital, cardiac, and skeletal malformations. Case Report A baby boy who was noticed to have ambiguous genitalia at birth was referred for genetic studies. Open in a separate window. Figure 1. Discussion Although initially 49,XXXXY pentasomy was considered a variant of Klinefelter syndrome, it is currently recognized as a separate clinical entity distinguished by facial features, multiple skeletal and cardiac defects and short stature.

References 1. Visootsak J, Graham JM. Klinefelter syndrome and other sex chromosomal aneuploidies. Orphanet J Rare Dis. with 49 Chromosomes.

Clin Genet. A rare case of ambiguous genitalia. Singapore Med J. Support Center Support Center. External link. Please review our privacy policy.

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