key: cord-0072590-qcf8a7dg
authors: Yadav, Amit Kumar; Wadia, Farokh; Gawhale, Sangeet; Panchal, Sameer; Talukder, Pritam; Mokashi, Mitali
title: Bilateral Severe Genu Varum in Dyggve-Melchior-Clausen Syndrome - A Case Report
date: 2021-08-03
journal: J Orthop Case Rep
DOI: 10.13107/jocr.2021.v11.i08.2378
sha: 044b6037ecc1dd759c79c2a9e3d2e4cf7653be1e
doc_id: 72590
cord_uid: qcf8a7dg

INTRODUCTION: Dyggve-Melchior-Clausen (DMC) syndrome was described in 1962 as an autosomal recessive type of spondyloepimetaphyseal dysplasia associated with mental retardation. Dymeclin (DYM) gene on chromosome 18q12.1 that encodes for DYM protein which is expressed in cartilage, bone, and brain is mutated in DMC. CASE REPORT: A 6 year -old male child presented with bilateral gradually progressive genu varum deformity of 4 years’ duration. There was no significant past medical and family history. A plain radiograph of his knee, pelvis, and spine shows some classical signs of skeletal dysplasia. A plain radiograph of the pelvis with both hips shows a classical semilunar, irregular lacy appearance around the iliac crest which is a pathognomonic radiological sign of this syndrome. CONCLUSION: The radiographic lacy appearance of iliac crests and generalized platyspondyly with double-humped end plates are pathognomonic of DMC.

confirm a diagnosis.

Clinical manifestations of DMC include pigeon-shaped chest, increased lumbar lordosis, broadening of the metaphysis, and brachydactyly [5] . Short neck with elevated shoulder joints, shortening of the upper extremity, and genu valgum or varum (Fig. 2b) were also present in most cases described in the literature. Rare manifestations include kyphoscoliosis, limitation of ex tension of joints, clinodactyly and camptodactyly of the fingers, prominent heels, flat feet or talipes equinovarus, bowing of femur, and tibia. Mild to severe mental retardation is present in all cases. The patients may also have delayed bone age, microcephaly, protruding abdomen, and generalized hirsutism. Tone, reflexes, and external genitalia are usually normal in DMC. The radiological findings include microcephaly with facial bone dysmorphism, small irregular epiphysis with often delayed ossification seen most commonly in proximal humerus and femur, and irregular metaphysis [6] . A plain radiograph of the pelvis with both hips shows a classical semilunar, irregular lacy appearance around the iliac crest which is a pathognomonic radiological sign of this syndrome (Fig. 2c) [7, 8] . The lacy appearance is due to bone deposition in a wavy pattern which appears at around 3-4 years of age and persists up to adulthood. There is an asymmetric bilateral widening of the sacroiliac joint. A radiograph of the dorsolumbar spine shows platyspondyly and central depression of vertebral bodies' endplates (Fig. 2a) . These double-hump-shaped endplates with the constricted central part are also characteristic of DMC syndrome. Other features are small or short ischium, hypoplastic acetabulum, hypoplastic femoral head and neck, medial beaking of the femoral neck, delayed pubic ramus synchondrosis, wide pubic symphysis, and bilateral dislocation of hip joints, odontoid hypoplasia, and atlantoaxial instability.

The closest differential diagnosis is Morquio's disease, but absent clouding of the cornea, valvular disease, organomegaly, and the presence of typical radiology support DMC. Joint stiffness is present in DMC, unlike the hyperlaxity seen in Morquio disease. The prognosis is better in DMC related to Morquio disease. We planned the patient for guided growth with eight plates but the patient lost to follow up due to coronavirus disease 2019 [10] .

The radiographic lacy appearance of iliac crests and generalized platyspondyly w ith double-humped end plates are pathognomonic of DMC and thus act as an easy pointer to diagnosis eliminating 435 genetic skeletal dysplasia's, directing appropriate genetic workup and counselling [9] .

DMC is an uncommon skeletal dysplasia. There is a good prognosis for general health and survival. The radiographic lacy appearance of iliac crests and generalized platyspondyly with double-humped end plates are pathognomonic of DMC. 

The radiographic lacy appearance of iliac crests is pathognomonic of DMC.

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