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Lenz Syndrome

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Lenz Syndrome" returned 0 free, full-text review articles. First 0 results:
Cenani-Lenz syndrome and other related syndactyly disorders due to variants in LRP4, GREM1/FMN1, and APC: Insight into the pathogenesis and the relationship to polyposis through the WNT and BMP antagonistic pathways.
Last Updated: Feb 06, 2020

Cenani-Lenz (C-L) syndrome is characterized by oligosyndactyly, metacarpal synostosis, phalangeal disorganization, and other variable facial and systemic features. Most cases are caused by homozygous and compound heterozygous missense and splice mutations of the LRP4 gene. Currently, ...

Cenani-Lenz syndrome: report of a new case and review of the literature.
Last Updated: Nov 06, 2019

A female child with Cenani-Lenz syndrome is described and the literature on this syndrome is reviewed.

Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
Last Updated: Nov 17, 2011

Lenz microphthalmia syndrome is a rare X-linked recessive condition first described by Lenz in 1955 and comprises of anophthalmia, microcephaly, mental retardation, external ear, digital, cardiac, skeletal, and urogenital anomalies. We present three brothers (ages 15 years, 9 years, ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Lenz Syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Lenz Syndrome" returned 9 free, full-text research articles. First few results:
Lenz-Majewski syndrome in a patient from Egypt.
Last Updated: Aug 03, 2020

Lenz-Majewski syndrome (LMS) is an extremely rare type of cutis laxa caused by dominant mutations in PTDSS1 gene. We report an Egyptian patient who presented with cutis laxa, brachydactyly, and progeroid features. LMS syndrome was suspected and a previously reported de novo heterozygous ...

Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene in skeletal cell lineages.
Last Updated: Jun 03, 2020

Lenz-Majewski syndrome (LMS) is characterized by osteosclerosis and hyperostosis of skull, vertebrae and tubular bones as well as craniofacial, dental, cutaneous, and digit abnormalities. We previously found that LMS is caused by dominant missense mutations in the   gene, which ...

Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly.
Last Updated: Apr 15, 2019

Cenani-Lenz Syndactyly (CLS) syndrome is a rare autosomal recessive disorder characterized by syndactyly and oligodactyly of fingers and toes, disorganization and fusion of metacarpals, metatarsals and phalanges, radioulnar synostosis and mesomelic shortness of the limbs, with lower ...

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9 Free Research Articles 34 Research Articles