A 6-year-old male child born of a non-consanguineous marriage admitted in the pediatrics emergency ward with the history of recurrent attacks of convulsion since 4 month of age. He was also suffering from frequent vomiting. Examination revealed that the child had characteristics features of angiofibromas on the face with butterfly distribution, hyperpigmented patches on forehead, hypopigmented ...

In this article, we review the major conceptual and clinical influences and trends in the history of couple therapy to date, and also chronicle the history of research on couple therapy. The evolving patterns in theory and practice are reviewed as having progressed through four distinctive phases: Phase I--Atheoretical Marriage Counseling Formation (1930-1963); Phase II--Psychoanalytic Experime...

This presentation focuses on the involvement of the Church in the HIV/AIDS awareness campaign. The Church believes in the sacredness of life in every person and in a human dignity that needs to be respected. Therefore, people with AIDS should not be condemned, avoided, or rejected. The Church also points out the importance of HIV/AIDS awareness education in explaining the meaning of human se...

In xeroderma pigmentosum, a rare genodermatosis, transmitted as an autosomal recessive disorder, excessive solar damage to the skin develops at an early age. The disease is characterized by cutaneous, ocular, neurological and oral changes. Oral features in the form of early development of squamous cell carcinoma, usually at the lower lip and tip of the tongue may be seen. The disorder is associ...

Fostering a sakinah family is the dream of all people who are building household, efforts to make it happen not an easy matter, because requires hard work and support from parties in family, both father, mother child. Not few families have problems even fail middle road, some members do sense responsibility carry out their obligations as they should family. For this reason, marriage guidance ne...

BACKGROUND Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene. Identification of spinal muscular atrophy carriers has important implications for individuals with a family history of the disorder and for genetic counseling. The aim of this study was to determine the frequency of carriers in a sample of the nonconsanguineous Brazili...

BACKGROUND Midwives are one of the most important health care providers and meeting their professional educational needs can be effective in maternal and child health promotion. AIM The aim of this study was to investigate the midwives' perspectives towards their educational needs. METHODS In this cross-sectional study which was conducted in 2012 in Sari, North of Iran, 223 midwives during ...