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Apert Syndrome : Comprehensive Care of the Patient and Family.

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Format:
Book
Author/Creator:
Meara, John G.
Contributor:
Meara
Series:
Medicine Series
Language:
English
Physical Description:
1 online resource (1013 pages)
Edition:
1st ed.
Place of Publication:
Cham : Springer, 2026.
Summary:
Apert syndrome - a rare genetic disorder characterized by craniofacial abnormalities, syndactyly (fusion of fingers and toes), and various health complications - presents unique challenges.
Notes:
Description based on publisher supplied metadata and other sources.
ISBN:
3-032-12551-0
OCLC:
1590083277

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