Summary (Text) Summary (XML) Create File Add to Clipboard Add to Collections Postnatal macrocephaly MedGen UID: 340230

Moderate postnatal growth retardation (Concept Id: C4024616) - MedGen - NCBI Warning: The NCBI web site requires JavaScript

Summary (Text) Summary (XML) Create File Add to Clipboard Add to Collections Postnatal-onset ichthyosiform erythroderma MedGen

ID: C1857641 • Finding Synonyms: Marked growth retardation; Postnatal growth retardation, severe; Severe postnatal growth deficiency; Severe postnatal growth failure   HPO: HP

Mild postnatal growth retardation (Concept Id: C1835580) - MedGen - NCBI Warning: The NCBI web site requires JavaScript

Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome (Concept Id: C4225254) - MedGen - NCBI Warning: The NCBI web site

mental and developmental health outcomes of children of mothers who had postnatal depression. Increased risk of

NICE Guideline NG3, Diabetes in pregnancy: management from preconception to the postnatal period NICE, 2019 UK

second decade. CS type II is characterized by growth failure at birth, with little or no postnatal neurologic development. Congenital cataracts

communicate. Seizures may develop during infancy or childhood. Additional common features include clubfeet, joint contractures, scoliosis, postnatal growth deficiency, increased risk

with a triad of characteristic findings: Congenital severe microcephaly Prenatal and postnatal growth restriction Congenital sensorineural

contractions of the elbows, wrists, and fingers. Other findings may include poor postnatal growth, strabismus, seizures, sleep

Abnormality of the nervous system See: Feature record | Search on this feature Growth abnormality Postnatal growth retardation Postnatal growth

the GeneReview: 3-M Syndrome 3-M syndrome is characterized by severe pre- and postnatal growth deficiency (final height

the protein is expressed in the inner ear during development and postnatal maturation and associates

protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory

Clinical characteristics. Simpson-Golabi-Behmel syndrome type 1 (SGBS1) is characterized by pre- and postnatal macrosomia; distinctive craniofacial features

of the nervous system See: Feature record | Search on this feature Growth abnormality Severe postnatal growth retardation Severe postnatal

ID: C0152421 Finding: Congenital Abnormality Ear malformation See: Feature record | Search on this feature Growth abnormality Postnatal growth retardation Postnatal growth

with the following clinical and radiographic findings. Clinical findings Pre- and postnatal growth failure Sagging, thin

99124 Concept ID: C0456070 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

a more severe lethal phenotype, osteocraniostenosis (OCS). KCS is characterized by proportionate short stature (typically postnatal onset), relative macrocephaly, large

hypertrichosis of other body parts. Other clinical features include feeding difficulties, prenatal and postnatal growth restriction, epilepsy, ophthalmologic

Abnormality of the nervous system See: Feature record | Search on this feature Growth abnormality Postnatal growth retardation Postnatal growth

4693 Concept ID: C0015934 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

and attention-deficit/hyperactivity disorder Ophthalmologic abnormalities (refractive errors and strabismus) Growth deficiency (postnatal short stature and

distention of the upper urinary tract) in association with impaired gastrointestinal motility Postnatal ultrasound examination or cystogram

Women’s Health. 2007; 52 :429–434. [ PubMed : 17826704 ] 17. Green K, Broome H, Mirabella J. Postnatal depression among mothers in

the symptomatic phase. The earliest signs, which are detected during embryonic and postnatal development and that

the GeneReview: 3-M Syndrome 3-M syndrome is characterized by severe pre- and postnatal growth deficiency (final height

NICE Guideline NG3, Diabetes in pregnancy: management from preconception to the postnatal period Consumer resources MalaCards

and head circumference are often at the lower range of normal; postnatal growth deficiency is profound

characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to

has a distinct mutant allele). (Orphanet) Summary Axial spondylometaphyseal dysplasia (SMDAX) is characterized by postnatal growth failure, including rhizomelic

whose mothers have normal thyroid function and who receive early and adequate postnatal treatment. Similarly, impaired hearing

humeri and femurs Fetal tachycardia (various forms of atrial tachycardia) Preterm delivery Postnatal findings Severe postnatal feeding

se slender and no rmal intelligence. It is characterized by pre- and postnatal growth retardation. Cervical spine

and radiographic findings and family history. Clinical findings Severe pre- and postnatal growth restriction Extreme microcephaly

Finding: Disease or Syndrome Ear malformation See: Feature record | Search on this feature Growth abnormality Mild postnatal growth retardation Mild postnatal

4693 Concept ID: C0015934 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

99124 Concept ID: C0456070 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

4693 Concept ID: C0015934 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

1% in group 2 and 10.2% in group 3. Thus, postnatal transmission was significantly lower

4693 Concept ID: C0015934 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

Concept ID: C2315100 Finding: Disease or Syndrome Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

congenital contractures with pterygia, onset of fractures in infancy or early childhood, postnatal short stature, severe limb

persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal growth deficiency. Other findings

5 SD below the mean before age one year Mild intrauterine growth restriction with postnatal catch up (Growth restriction

individuals. The other half had primary microcephaly (OFC <-2 SD). Mild-to-severe postnatal microcephaly evolved rapidly during

Department of Labor, Occupational Safety and Health Administration P3 (and similar) postnatal day number PACT Prevent

A recent study comparing diethylstilbestrol-exposed CCA cases to diethylstilbestrol-controls did not identify postnatal factors that influenced the

deficient infantile parkinsonism with motor delay; however, no levodopa trials in the early postnatal period of infants

spurt Fetal growth restriction Mild intrauterine growth retardation Moderate intrauterine growth retardation Severe intrauterine growth retardation Postnatal growth retardation Mild postnatal

persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal growth deficiency. Other findings

A recent study comparing diethylstilbestrol-exposed CCA cases to diethylstilbestrol-controls did not identify postnatal factors that influenced the

7 Distinguishing Clinical Features BLM ( RECQL3 ) Bloom syndrome   2 AR 1%-5% Childhood Severe pre- & postnatal growth deficiency, immune abnormalities

18–21). The day of parturition was considered to be postnatal day (PND) 0. On

joint limitation or laxity, and soft, lax skin. Growth abnormalities include prenatal growth deficiency, postnatal poor weight gain, and

role in internal organ development and function during pre- and postnatal life. This gene is

Physical features (in ~75% of affected persons) Prenatal and/or postnatal short stature Abnormal skin

Neurologic: brain atrophy, peripheral neuropathy (mineral and vitamin deficiencies) Obstetric: antenatal and postnatal complications Psychiatric: depression, impaired

Clipboard Add to Collections P2 Hydronephrosis MedGen UID: 887766 • Concept ID: C4054279 • Finding Definition Postnatal Hydronephrosis with the

GLYCAN EXTENSIONS Many glycan extensions are regulated during embryogenesis and in the postnatal period as part of

to thrive in infancy as a result of severe postnatal feeding difficulties; short stature

4693 Concept ID: C0015934 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

receptor for insulin-like growth factor I show intrauterine growth retardation and postnatal growth failure, resulting in

with associated fasting hypoglycemia and postprandial hyperglycemia), severe prenatal growth restriction and postnatal growth failure, hypotonia and

persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal growth deficiency. Other findings

reading time: 12 minutes Summary Clinical characteristics. Emanuel syndrome is characterized by pre- and postnatal growth deficiency, microcephaly, hypotonia

twofold increase in the respective TCPP exposure concentrations in feed. At postnatal day (PND) 1, there

health consequences of mother and newborn. [2] Function Timing of Postnatal Visits In April

persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal growth deficiency. Other findings

99124 Concept ID: C0456070 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

23 minutes Summary Clinical characteristics. 3-M syndrome is characterized by severe pre- and postnatal growth deficiency (final height

R. Stein; Multidisciplinary consensus on the classification of prenatal and postnatal urinary tract dilation (UTD

99124 Concept ID: C0456070 Finding: Pathologic Function Growth abnormality See: Feature record | Search on this feature Postnatal growth retardation Postnatal growth

4/26 (15%) Nuchal redundancy / cystic hygroma 4/26 (15%) Noted either on prenatal imaging or postnatal physical exam 1. Not

ATRX XL Hypotonia Coarse facial features Alpha-thalassemia & HbH inclusion bodies Genital anomalies Microcephaly common Postnatal growth deficiency Kleefstra syndrome

third trimester can show an enlarged bladder (megacystis) and dilated upper urinary tracts (hydronephrosis). Postnatal imaging by ultrasonography and

syndrome A) is characterized by a progeroid appearance, pre- and postnatal growth restriction, moderate to

with hematologic problems have been reported thus far. Growth. Intrauterine growth restriction (IUGR) and postnatal growth delay are occasionally

in a proband with the following: Distorting, progressive overgrowth, typically of postnatal onset, often resulting in

the long arm of chromosome 20 presenting with severe pre- and postnatal growth restriction and

and intermittent seizures [ Bosley et al 2014 ]. Although head circumference is normal at birth, severe progressive postnatal microcephaly develops [ Bosley et

AOI) and III (AOIII) and Piepkorn osteochondrodysplasia (POCD). SCT syndrome is characterized by postnatal disproportionate short stature, scoliosis

second decade. CS type II is characterized by growth failure at birth, with little or no postnatal neurologic development. Congenital cataracts

hypertrichosis of other body parts. Other clinical features include feeding difficulties, prenatal and postnatal growth restriction, epilepsy, ophthalmologic

to thrive in infancy as a result of severe postnatal feeding difficulties; short stature

second decade. CS type II is characterized by growth failure at birth, with little or no postnatal neurologic development. Congenital cataracts

the enzyme 7-dehydrocholesterol (7-DHC) reductase. It is characterized by prenatal and postnatal growth restriction, microcephaly, moderate

second decade. CS type II is characterized by growth failure at birth, with little or no postnatal neurologic development. Congenital cataracts

count or WHO clinical staging, and that the risk of postnatal transmission is reduced with

drug resistance will need to be monitored. 4.2. Antenatal, perinatal and postnatal care Routine provider-initiated

the GeneReview: 3-M Syndrome 3-M syndrome is characterized by severe pre- and postnatal growth deficiency (final height

enhanced treatment options. Macroglossia and macrosomia are generally present at birth but may have postnatal onset. Growth rate slows

prominent forehead with frontal bossing, and frequently body asymmetry. This is typically followed by postnatal growth failure, and

problems are observed in some children with SALL1 -TBS, especially attention-deficit/hyperactivity disorder. Postnatal growth deficiency. This poorly

SRS) 11p15.5 H19/IGR2 :IG DMR LOM  8 SGA  9 & relative macrocephaly at birth Postnatal growth failure Prominent forehead

and electrolyte imbalance in severely affected infants may be critical during the postnatal period. Nutritional support including

gland In CAIS, but not in PAIS: possible reduction in postnatal (0-3 months) surge