We describe a training program to teach applied behavior analysis (ABA) knowledge competencies to paraprofessional staff (N = 47) at a habilitation services agency for adults with developmental disabilities. Before and following training, staff completed. TIP 56: Addressing the Specific Behavioral Health Needs of Men This guide addresses specific treatment needs of adult men living with substance use disorders. It reviews gender-specific research and best practices, such as common patterns of substance use among.
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Dialectical Behavioral Therapy Dbt Techniques
Some people with 47, XXY do not have any noticeable signs or symptoms (features) associated with the chromosome variation. Others may have features that range from mild to severe.[1][2]
In general male babies and young boys with 47, XXY are not very different from babies and young boys with 46, XY. Some may have slightly longer legs, weaker muscles, delayed development of motor skills, and learning and/or language problems. Puberty and adulthood is when differences may become more clear. One of the most common features shared by males with 47, XXY is hypogonadism, which means the testes do not produce enough testosterone. Other than a small period in infancy, testosterone production is not important until puberty. Low testosterone may cause some boys with 47, XXY to have delayed or incomplete puberty, as well as may worsen concentration, mood, and behavioral problems. For others, the low testosterone may not cause noticeable symptoms until adulthood when low sexual drive and tiredness may develop and continue to worsen with age. For some men, infertility caused by no or low sperm count may be the first detected symptom.[1][2]
Many but not all males with 47, XXY may develop signs and symptoms (features) of Klinefelter syndrome (KS) during their teen and adult years. KS is the name of a collection of features that include decreased testosterone production (primary hypogonadism), small testes, enlarged breast tissue (gynecomastia), tall stature, long legs, wide hips, learning disabilities, behavioral problems, and social relational problems. KS can also be caused by other sex chromosome variations.[1][2]
In general male babies and young boys with 47, XXY are not very different from babies and young boys with 46, XY. Some may have slightly longer legs, weaker muscles, delayed development of motor skills, and learning and/or language problems. Puberty and adulthood is when differences may become more clear. One of the most common features shared by males with 47, XXY is hypogonadism, which means the testes do not produce enough testosterone. Other than a small period in infancy, testosterone production is not important until puberty. Low testosterone may cause some boys with 47, XXY to have delayed or incomplete puberty, as well as may worsen concentration, mood, and behavioral problems. For others, the low testosterone may not cause noticeable symptoms until adulthood when low sexual drive and tiredness may develop and continue to worsen with age. For some men, infertility caused by no or low sperm count may be the first detected symptom.[1][2]
Many but not all males with 47, XXY may develop signs and symptoms (features) of Klinefelter syndrome (KS) during their teen and adult years. KS is the name of a collection of features that include decreased testosterone production (primary hypogonadism), small testes, enlarged breast tissue (gynecomastia), tall stature, long legs, wide hips, learning disabilities, behavioral problems, and social relational problems. KS can also be caused by other sex chromosome variations.[1][2]
