Familial juvenile hyperuricemic nephropathy (FJHN) and medullary cystic kidney disease type 2 (MCKD2) are autosomal dominant disorders characterized by juvenile hyperuricemia of the underexcretion type, juvenile gout and chronic renal failure in the adult. FJHN/MCKD2 constitute diseases caused by mutations of the human uromodulin (UMOD) gene that encodes uromodulin, the most abundant glycoprote...

OBJECTIVE To determine the prevalence of dry eye symptoms and signs in children with juvenile idiopathic arthritis (JIA). PATIENTS AND METHODS A total of 192 children with JIA: 48 oligo-, 39 extended oligo-, 79 polyarthritis, and 26 with other types of arthritis (eight juvenile spondyloarthritis, five juvenile psoriatic arthritis, three mixed connective tissue diseases, two systemic onset art...


 The purpose of this study was to describe the role Jami Al-Muhajirin Mosque Youth Organization in Preventing Juvenile Delinquency Rw 20 Central Depok II. method used is a qualitative and included type case research. Data collection procedures that researchers do by observations, interviews documentation. results og research thesis show forms Iiare there are groups teenagers who gamble on...

BACKGROUND This systematic review is the first step in a study investigating the resilience methods and processes in families of children with juvenile idiopathic arthritis. In particular, this review will focus on chronic or persistent pain, as a common symptom of juvenile idiopathic arthritis, which is the most common rheumatic disease in childhood. The experience of persistent pain can add t...

Objective: This clinical study was conducted to evaluate a cartilage repair procedure of transplanting particulated juvenile cartilage tissue allograft (DeNovo NT Natural Tissue Graft). Design: A multi-center, prospective, single arm, 25-subject clinical study was designed to evaluate clinical outcomes such as IKDC and KOOS scores, as well as extent and quality of repair with MRI and optional b...

Sunita Gupta1, Sinny Goel2, Sujoy Ghosh3, Aarti Singh4 1Professor and Head, Department of Oral Medicine and Radiology, Maulana Azad Institute of Dental Sciences, New Delhi, India, 2Postgraduate Student, Department of Oral Medicine and Radiology, Maulana Azad Institute of Dental Sciences, New Delhi, India, 3Associate Professor, Department of Oral Medicine and Radiology, Maulana Azad Institute of...

The aim of this paper was to present a brief case report of Trabecular Juvenile Ossifying Fibroma (WHO-type) (TJOF WHO-type), and compare the clinical and histopathological findings with current literature in order to seek clarification of the nature and behavior of the lesion. Conclusions: The TJOF (WHO-type) is a rare fibro-osseous begnin injury with biologic aggressive behavior, and unknown ...

We report the cases of 5 adolescents with human T lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis, acquired in all but 1 case from the mother. The first symptom in all patients was difficulty in running, which was present for many years before the final diagnosis was made. Follow-up showed an indolent progression, regardless of treatment strategy.

Postembryonic shoot development in maize (Zea mays L.) is divided into a juvenile vegetative phase, an adult vegetative phase, and a reproductive phase that differ in the expression of many morphological traits. A reduction in the endogenous levels of bioactive gibberellins (GAs) conditioned by any one of the dwarf1, dwarf3, dwarf5, or anther ear1 mutations in maize delays the transition from j...

Inadequate pancreatic β cell function underlies type 1 and type 2 diabetes mellitus. Strategies to expand functional cells have focused on discovering and controlling mechanisms that limit the proliferation of human β cells. Here, we developed an engraftment strategy to examine age-associated human islet cell replication competence and reveal mechanisms underlying age-dependent decline of β cel...