Split-hand/foot malformation type 1 with sensorineural hearing loss (SHFM1D): A case report
Split-hand/split-foot malformation (SHFM), also known as ectrodactyly is a rare genetic condition characterized by malformation of the limbs with median clefts of the hands and feet and aplasia/hypoplasia of the phalanges, metacarpals, and metatarsals. It has a prevalence of 1:10,000-1:90,000 worldw...
Saved in:
Main Authors: | Chandra Madhur Sharma (Author), Deepti Sharma (Author), Manoj K Meghwani (Author), Ravi P Agrawal (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Autosomal recessive split-hand/split-foot malformation
by: Monojit Mondal, et al.
Published: (2016) -
Sensorineural hearing loss in Kawasaki disease
by: Varun Aggarwal, et al.
Published: (2016) -
Sensorineural hearing loss in Kawasaki disease
by: Mahmood Dhahir Al-Mendalawi
Published: (2016) -
PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation
by: Brittany T. Truong, et al.
Published: (2023) -
Advancements in prevention and intervention of sensorineural hearing loss
by: Hongmiao Ren, et al.
Published: (2022)