Delayed Presentation of Rickets in a Child with Labyrinthine Aplasia, Microtia and Microdontia (LAMM) Syndrome.

dc.contributor.authorSingh, Ankur
dc.contributor.authorTekin, Mustafa
dc.contributor.authorFalcone, Michelle
dc.contributor.authorKapoor, Seema
dc.date.accessioned2016-01-25T11:22:48Z
dc.date.available2016-01-25T11:22:48Z
dc.date.issued2014-11
dc.description.abstractBackground: Labyrinthine Aplasia, Microtia and Microdontia (LAMM) syndrome is characterized by the complete absence of inner ear structures (Michel aplasia), microtia and microdontia. Hypophosphatemic rickets results from defects in the renal tubular reabsorption of filtered phosphate. Case characteristics: 13-year-old Indian girl presented with deafness since infancy and progressive wrist widening and genu valgum for last one year. Observation: Homozygous novel missense mutation in fibroblast growth factor 3. Message: LAMM syndrome and hypophosphatemic rickets may be associated.en_US
dc.identifier.citationSingh Ankur, Tekin Mustafa, Falcone Michelle, Kapoor Seema. Delayed Presentation of Rickets in a Child with Labyrinthine Aplasia, Microtia and Microdontia (LAMM) Syndrome. Indian Pediatrics. 2014 Nov; 51(11): 919-920.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/170912
dc.language.isoenen_US
dc.source.urihttps://www.indianpediatrics.net/nov2014/nov-919-920.htmen_US
dc.subjectDeafnessen_US
dc.subjectFibroblast growth factor receptor-3en_US
dc.subjectHypophosphatemic ricketsen_US
dc.titleDelayed Presentation of Rickets in a Child with Labyrinthine Aplasia, Microtia and Microdontia (LAMM) Syndrome.en_US
dc.typeArticleen_US
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
ip2014v51n11p919.pdf
Size:
36.65 KB
Format:
Adobe Portable Document Format
Description:
Case Reports
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: