health
William's Syndrome
Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and cardiovascular abnormalities.
Posted September 23, 2022 by Anusha ‐ 2 min read
Plummer Vinson Syndrome
Plummer–Vinson syndrome is a rare disease characterized by difficulty swallowing, iron-deficiency anemia, glossitis, cheilosis and esophageal webs.
Posted September 23, 2022 by Anusha ‐ 2 min read
⌖ diseases treatments syndromes disorders plummer-vinson-syndrome health
Parry Romberg Syndrome
Parry-Romberg syndrome is a rare, acquired disorder characterized by slowly progressive shrinkage (atrophy) of the skin and soft tissues of half of the face (hemifacial atrophy).
Posted September 23, 2022 by Anusha ‐ 3 min read
⌖ diseases treatments syndromes disorders progressive-facial-hemiatrophy progressive-hemifacial-atrophy health hemifacial-atrophy parry-romberg-syndrome prs romberg-syndrome
Chediak Higashi Syndrome
Albinism is a lack of color in the skin, hair, and eyes. Chediak-Higashi syndrome (CHS) is an extremely rare form of partial albinism that’s accompanied by problems with the immune and nervous systems.
Posted September 23, 2022 by Anusha ‐ 2 min read
⌖ diseases treatments chediak-higashi--syndrome syndromes disorders health
Nevoid Basal Cell Carcinoma Syndrome
Nevoid basal-cell carcinoma syndrome (NBCCS) is an inherited medical condition involving defects within multiple body systems such as the skin, nervous system, eyes, endocrine system, and bones. People with this syndrome are particularly prone to developing a common and usually non-life-threatening form of non-melanoma skin cancer.
Posted September 24, 2022 by Anusha ‐ 2 min read
⌖ diseases treatments syndromes disorders health nevoid-basal-cell-carcinoma-syndrome