Peters-plus syndrome · Medical condition · YYNN

Peters-plus syndrome

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Medical condition

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Subject of
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Corrigendum to: ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome

scientific article published on 12 June 2020

ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome

scientific article published on 01 December 2019

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Peters-plus syndrome or Krause–Kivlin syndrome is a hereditary syndrome defined by Peters' anomaly, dwarfism and intellectual disability.

Instance of

developmental defect during embryogenesis

class of disease

Subclass of

multiple congenital anomalies/dysmorphic syndrome-intellectual disability

congenital disorder of glycosylation with cardiac malformation as a major feature

non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature

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