Barraquer–Simons syndrome
Acquired partial lipodystrophy, or Barraquer-Simons syndrome, is characterised by the association of lipoatrophy of the upper part of the body and lipohypertrophy of the thighs
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Barraquer–Simons syndrome
Summary
Barraquer–Simons syndrome is a developmental defect during embryogenesis[1]. It draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #125 of 308).[2]
Key Facts
- Barraquer–Simons syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Barraquer–Simons syndrome's instance of is recorded as class of disease[4].
- Luis Barraquer Roviralta is named after Barraquer–Simons syndrome[5].
- Arthur Simons is named after Barraquer–Simons syndrome[6].
- Barraquer–Simons syndrome is a type of lipodystrophy[7].
- Barraquer–Simons syndrome is a type of developmental anomaly of metabolic origin[8].
- Barraquer–Simons syndrome is a type of partial lipodystrophy[9].
- Barraquer–Simons syndrome is a type of acquired lipodystrophy[10].
- Barraquer–Simons syndrome is a type of progeroid syndrome[11].
- Barraquer–Simons syndrome's NCI Thesaurus ID is recorded as C129723[12].
- Barraquer–Simons syndrome's health specialty is recorded as endocrinology[13].
- Barraquer–Simons syndrome's genetic association is recorded as LMNB2[14].
- Barraquer–Simons syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79087[15].
Why It Matters
Barraquer–Simons syndrome draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #125 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[16] It is known by 11 alternative names across languages and contexts.[17]