Juvenile CML
Juvenile myelomonocytic leukemia.
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- Juvenile hyaline fibromatosis
A genetic disorder characterized by multiple subcutaneous nodules and gingival hypertrophy (overgrowth of the gums) beginning in the first few years of life and, later, joint contractures. There are deposits of hyaline (glassy) material in the skin. The disease is inherited as an autosomal recessive condition. The gene for the disease is on chromosome 4q21.21. […]
- Juvenile laryngeal papillomatosis
A condition characterized by the emergence of numerous warty growths on the vocal cords in children and young adults. A baby can contract juvenile laryngeal papillomatosis by being infected with the human papillomavirus (HPV) during birth through the vaginal canal of a mother who has genital warts. Treatment usually involves surgical excision. Recurrences of laryngeal […]
- Juvenile myelomonocytic leukemia
Abbreviated JMML. A rare cancer of the myeloid cells in the bone marrow, accounting for less than 1% of all childhood leukemia. JMML is most common in children under four years of age, especially those with genetic disorders called neurofibromatosis 1 (NF1) and Noonan syndrome. Up to 14% of cases of JMML occur in children […]
- Juvenile polyposis
An autosomal dominant disorder in which polyps develop throughout the gastrointestinal tract in the first decade or two of life. People with the disease are at increased risk for developing gastrointestinal cancers. There can also be diarrhea, GI bleeding, and protein-losing from the intestinal wall. The majority of cases of juvenile polyposis appear sporadic with […]
- Juvenile polyposis syndrome
An autosomal dominant disorder in which polyps develop throughout the gastrointestinal tract in the first decade or two of life. People with the disease are at increased risk for developing gastrointestinal cancers. Abbreviated JPS. There can also be diarrhea, GI bleeding, and protein-losing from the intestinal wall. JPS is clearly heterogeneous (more than one entity) […]