Seckel syndrome、Seckel syndrome、Poland syndrome在PTT/mobile01評價與討論，在ptt社群跟網路上大家這樣說
Seckel syndrome關鍵字相關的推薦文章
Seckel syndrome在Seckel Syndrome - NORD (National Organization for Rare ...的討論與評價
Seckel syndrome is rare genetic condition with slow growth before birth (intrauterine growth restriction) resulting in low birth weight.
Seckel syndrome在Seckel syndrome - Wikipedia的討論與評價
Seckel syndrome, or microcephalic primordial dwarfism is an extremely rare congenital nanosomic disorder. Inheritance is autosomal recessive.
Seckel syndrome在Seckel syndrome - Genetic and Rare Diseases Information ...的討論與評價
Medical Terms Other Names Learn More:HPO ID Cachexia Wasting syndrome 0004326 Clinodactyly of the 5th finger Permanent curving of the pinkie finger 0004209 Craniosynostosis ‑ ‑‑> 0001363
Seckel syndrome在ptt上的文章推薦目錄
Seckel syndrome在Seckel syndrome - Orphanet的討論與評價
A rare form of microcephalic primordial dwarfism characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly, a typical dysmorphic face ( ...
Seckel syndrome在Seckel Syndrome - an overview | ScienceDirect Topics的討論與評價
Seckel (SCKL) syndrome, sometimes called “bird-headed dwarfism,” is an autosomal recessive developmental disorder characterized by marked growth failure and ...
Seckel syndrome在OMIM Entry - # 210600 - SECKEL SYNDROME 1; SCKL1的討論與評價
Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with mental retardation, ...
Seckel syndrome在Verification and rectification of cell type-specific splicing of a ...的討論與評價
Seckel syndrome (SS, OMIM: 210600) is a spectrum of congenital disorders that mainly exhibit intrauterine growth defects resulting in severe ...
Seckel syndrome在Seckel Syndrome and Primordial Dwarfism - Verywell Health的討論與評價
Seckel syndrome is an inherited form of primordial dwarfism, meaning that an infant starts out very small and fails to grow normally after ...
Seckel syndrome在A Child with Seckel Syndrome and Arterial Stenosis: Case ...的討論與評價
Background: Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is characterized by dysmorphic features, ...
Seckel syndrome在POMS: DI 23022.296 - Seckel Syndrome - 08/28/2020 - Social ...的討論與評價
Seckel syndrome (SCKL) is a rare genetic disorder characterized by growth delays prior to birth (intrauterine growth retardation), ...