Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.

Kenny-Caffey syndrome without the CATCH 22 deletion.

Kenny-Caffey syndrome. Case report and literature review.

Kenny-Caffey Syndrome is a rare syndrome characterized by growth retardation, uniformly small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia possibly with tetany at an early age, hyperphosphatemia, ocular abnormalities, and normal intelligence. We report a child with Kenny-Caffey Syndrome and idiopathic hypoparathyroidism and present a review of the...

Contraction and decomposition matrices for vacuum diagrams

Tensor reduction of vacuum diagrams uses contraction and decomposition matrices. We present general recurrence relations for the calculation of those matrices and an explicit formula for the 3-loop decomposition matrix and its determinant. Email: Kenny [email protected] Email: [email protected] 1

Enumerating Molecules

This report is a comprehensive review of the field of molecular enumeration from early isomer counting theories to evolutionary algorithms that design molecules in silico. The core of the review is a detail account on how molecules are counted, enumerated, and sampled. The practical applications of molecular enumeration are also reviewed for chemical information, structure elucidation, molecula...

Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene

BACKGROUND Hypoparathyroidism in children is a heterogeneous group with diverse genetic etiologies. To aid clinicians in the investigation and management of children with hypoparathyroidism, we describe the phenotype of a 6-year-old child with hypoparathyroidism and short stature diagnosed with Kenny-Caffey syndrome (KCS) Type 2 and the subsequent response to growth hormone (GH) treatment. CA...